esv3585870

Organism: Homo sapiens

Study:estd214 (1000 Genomes Consortium Phase 3)
Variant Type:inversion
Method Type:Sequencing
Submitted on:GRCh37

Variant Calls:2,240
Validation:Not tested
Clinical Assertions: No
Region Size:661

Publication(s):1000 Genomes Project Consortium et al. 2015

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 169 SVs from 42 studies. See in: genome view

Remapped(Score: Perfect):43,593,558-43,594,340

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3585870	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
esv3585870	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000001.10	Chr1	44,059,290 (-61, +61)	44,059,950 (-61, +61)

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
essv9921759	inversion	SAMN00004622	Sequencing	Read depth and paired-end mapping	Heterozygous	2,214
essv9921760	inversion	SAMN00004623	Sequencing	Read depth and paired-end mapping	Homozygous	2,667
essv9921761	inversion	SAMN00004625	Sequencing	Read depth and paired-end mapping	Heterozygous	2,591
essv9921762	inversion	SAMN00004626	Sequencing	Read depth and paired-end mapping	Heterozygous	2,931
essv9921763	inversion	SAMN00004627	Sequencing	Read depth and paired-end mapping	Homozygous	2,692
essv9921764	inversion	SAMN00004628	Sequencing	Read depth and paired-end mapping	Homozygous	2,684
essv9921765	inversion	SAMN00004629	Sequencing	Read depth and paired-end mapping	Heterozygous	2,200
essv9921766	inversion	SAMN00004631	Sequencing	Read depth and paired-end mapping	Heterozygous	2,737
essv9921767	inversion	SAMN00004632	Sequencing	Read depth and paired-end mapping	Homozygous	2,666
essv9921768	inversion	SAMN00004633	Sequencing	Read depth and paired-end mapping	Homozygous	2,664
essv9921769	inversion	SAMN00004634	Sequencing	Read depth and paired-end mapping	Homozygous	2,737
essv9921770	inversion	SAMN00004635	Sequencing	Read depth and paired-end mapping	Homozygous	2,821
essv9921771	inversion	SAMN00004636	Sequencing	Read depth and paired-end mapping	Homozygous	2,698
essv9921772	inversion	SAMN00004637	Sequencing	Read depth and paired-end mapping	Homozygous	2,609
essv9921773	inversion	SAMN00004638	Sequencing	Read depth and paired-end mapping	Homozygous	2,504
essv9921774	inversion	SAMN00004639	Sequencing	Read depth and paired-end mapping	Homozygous	2,703
essv9921775	inversion	SAMN00004640	Sequencing	Read depth and paired-end mapping	Homozygous	2,393
essv9921776	inversion	SAMN00004641	Sequencing	Read depth and paired-end mapping	Heterozygous	2,942
essv9921777	inversion	SAMN00004642	Sequencing	Read depth and paired-end mapping	Homozygous	2,702
essv9921778	inversion	SAMN00004643	Sequencing	Read depth and paired-end mapping	Homozygous	2,552
essv9921779	inversion	SAMN00006337	Sequencing	Read depth and paired-end mapping	Heterozygous	2,882
essv9921780	inversion	SAMN00006338	Sequencing	Read depth and paired-end mapping	Homozygous	2,748
essv9921781	inversion	SAMN00004644	Sequencing	Read depth and paired-end mapping	Heterozygous	2,699
essv9921782	inversion	SAMN00006339	Sequencing	Read depth and paired-end mapping	Homozygous	2,741
essv9921783	inversion	SAMN00006340	Sequencing	Read depth and paired-end mapping	Homozygous	2,731
essv9921784	inversion	SAMN00006341	Sequencing	Read depth and paired-end mapping	Homozygous	2,683
essv9921785	inversion	SAMN00006343	Sequencing	Read depth and paired-end mapping	Homozygous	2,433
essv9921786	inversion	SAMN00006344	Sequencing	Read depth and paired-end mapping	Heterozygous	2,768
essv9921787	inversion	SAMN00004645	Sequencing	Read depth and paired-end mapping	Heterozygous	2,148
essv9921788	inversion	SAMN00004646	Sequencing	Read depth and paired-end mapping	Heterozygous	2,568
essv9921789	inversion	SAMN00004647	Sequencing	Read depth and paired-end mapping	Homozygous	2,660
essv9921790	inversion	SAMN00004648	Sequencing	Read depth and paired-end mapping	Homozygous	2,529
essv9921791	inversion	SAMN00004649	Sequencing	Read depth and paired-end mapping	Homozygous	2,793
essv9921792	inversion	SAMN00004650	Sequencing	Read depth and paired-end mapping	Homozygous	2,682
essv9921793	inversion	SAMN00004651	Sequencing	Read depth and paired-end mapping	Homozygous	2,831
essv9921794	inversion	SAMN00004654	Sequencing	Read depth and paired-end mapping	Homozygous	2,593
essv9921795	inversion	SAMN00004655	Sequencing	Read depth and paired-end mapping	Heterozygous	2,454
essv9921796	inversion	SAMN00004656	Sequencing	Read depth and paired-end mapping	Homozygous	2,595
essv9921797	inversion	SAMN00004657	Sequencing	Read depth and paired-end mapping	Homozygous	2,763
essv9921798	inversion	SAMN00004658	Sequencing	Read depth and paired-end mapping	Homozygous	2,650
essv9921799	inversion	SAMN00004659	Sequencing	Read depth and paired-end mapping	Heterozygous	2,876
essv9921800	inversion	SAMN00004660	Sequencing	Read depth and paired-end mapping	Homozygous	2,465
essv9921801	inversion	SAMN00004661	Sequencing	Read depth and paired-end mapping	Homozygous	2,731
essv9921802	inversion	SAMN00004663	Sequencing	Read depth and paired-end mapping	Homozygous	2,670
essv9921803	inversion	SAMN00004664	Sequencing	Read depth and paired-end mapping	Heterozygous	2,739
essv9921804	inversion	SAMN00004666	Sequencing	Read depth and paired-end mapping	Homozygous	2,758
essv9921805	inversion	SAMN00004667	Sequencing	Read depth and paired-end mapping	Heterozygous	2,709
essv9921806	inversion	SAMN00004668	Sequencing	Read depth and paired-end mapping	Heterozygous	2,231
essv9921807	inversion	SAMN00004669	Sequencing	Read depth and paired-end mapping	Homozygous	2,753
essv9921808	inversion	SAMN00009088	Sequencing	Read depth and paired-end mapping	Homozygous	2,888
essv9921809	inversion	SAMN00004672	Sequencing	Read depth and paired-end mapping	Homozygous	2,782
essv9921810	inversion	SAMN00004674	Sequencing	Read depth and paired-end mapping	Homozygous	2,809
essv9921811	inversion	SAMN00004675	Sequencing	Read depth and paired-end mapping	Homozygous	2,600
essv9921812	inversion	SAMN00006345	Sequencing	Read depth and paired-end mapping	Homozygous	2,777
essv9921813	inversion	SAMN00004676	Sequencing	Read depth and paired-end mapping	Homozygous	2,580
essv9921814	inversion	SAMN00016965	Sequencing	Read depth and paired-end mapping	Homozygous	2,566
essv9921815	inversion	SAMN00016966	Sequencing	Read depth and paired-end mapping	Homozygous	2,448
essv9921816	inversion	SAMN00016967	Sequencing	Read depth and paired-end mapping	Heterozygous	2,522
essv9921817	inversion	SAMN00016969	Sequencing	Read depth and paired-end mapping	Homozygous	2,443
essv9921818	inversion	SAMN00016970	Sequencing	Read depth and paired-end mapping	Homozygous	2,824
essv9921819	inversion	SAMN00016971	Sequencing	Read depth and paired-end mapping	Heterozygous	2,465
essv9921820	inversion	SAMN00016972	Sequencing	Read depth and paired-end mapping	Homozygous	2,408
essv9921821	inversion	SAMN00016973	Sequencing	Read depth and paired-end mapping	Homozygous	2,813
essv9921822	inversion	SAMN00016974	Sequencing	Read depth and paired-end mapping	Homozygous	2,666
essv9921823	inversion	SAMN00016975	Sequencing	Read depth and paired-end mapping	Homozygous	2,531
essv9921824	inversion	SAMN00016976	Sequencing	Read depth and paired-end mapping	Heterozygous	2,756
essv9921825	inversion	SAMN00016977	Sequencing	Read depth and paired-end mapping	Homozygous	2,562
essv9921826	inversion	SAMN00016978	Sequencing	Read depth and paired-end mapping	Homozygous	2,554
essv9921827	inversion	SAMN00016979	Sequencing	Read depth and paired-end mapping	Heterozygous	2,879
essv9921828	inversion	SAMN00016980	Sequencing	Read depth and paired-end mapping	Heterozygous	2,748
essv9921829	inversion	SAMN00016981	Sequencing	Read depth and paired-end mapping	Homozygous	2,774
essv9921830	inversion	SAMN00006346	Sequencing	Read depth and paired-end mapping	Homozygous	2,602
essv9921831	inversion	SAMN00006347	Sequencing	Read depth and paired-end mapping	Homozygous	2,456
essv9921832	inversion	SAMN00004678	Sequencing	Read depth and paired-end mapping	Heterozygous	2,465
essv9921833	inversion	SAMN00004679	Sequencing	Read depth and paired-end mapping	Heterozygous	2,446
essv9921834	inversion	SAMN00006348	Sequencing	Read depth and paired-end mapping	Homozygous	2,664
essv9921835	inversion	SAMN00006349	Sequencing	Read depth and paired-end mapping	Homozygous	2,741
essv9921836	inversion	SAMN00004680	Sequencing	Read depth and paired-end mapping	Homozygous	2,630
essv9921837	inversion	SAMN00006350	Sequencing	Read depth and paired-end mapping	Homozygous	2,652
essv9921838	inversion	SAMN00004681	Sequencing	Read depth and paired-end mapping	Heterozygous	2,727
essv9921839	inversion	SAMN00006351	Sequencing	Read depth and paired-end mapping	Heterozygous	2,773
essv9921840	inversion	SAMN00006352	Sequencing	Read depth and paired-end mapping	Homozygous	2,799
essv9921841	inversion	SAMN00006353	Sequencing	Read depth and paired-end mapping	Homozygous	2,837
essv9921842	inversion	SAMN00006354	Sequencing	Read depth and paired-end mapping	Homozygous	2,703
essv9921843	inversion	SAMN00009089	Sequencing	Read depth and paired-end mapping	Heterozygous	2,585
essv9921844	inversion	SAMN00009091	Sequencing	Read depth and paired-end mapping	Homozygous	2,832
essv9921845	inversion	SAMN00009092	Sequencing	Read depth and paired-end mapping	Homozygous	2,808
essv9921846	inversion	SAMN00006357	Sequencing	Read depth and paired-end mapping	Homozygous	2,740
essv9921847	inversion	SAMN00006358	Sequencing	Read depth and paired-end mapping	Homozygous	2,757
essv9921848	inversion	SAMN00006359	Sequencing	Read depth and paired-end mapping	Homozygous	2,753
essv9921849	inversion	SAMN00004682	Sequencing	Read depth and paired-end mapping	Homozygous	2,758
essv9921850	inversion	SAMN00006360	Sequencing	Read depth and paired-end mapping	Homozygous	2,737
essv9921851	inversion	SAMN00006361	Sequencing	Read depth and paired-end mapping	Homozygous	2,773
essv9921852	inversion	SAMN00006362	Sequencing	Read depth and paired-end mapping	Heterozygous	2,917
essv9921853	inversion	SAMN00006363	Sequencing	Read depth and paired-end mapping	Homozygous	2,862
essv9921854	inversion	SAMN00006364	Sequencing	Read depth and paired-end mapping	Homozygous	2,776
essv9921855	inversion	SAMN00006365	Sequencing	Read depth and paired-end mapping	Homozygous	2,690
essv9921856	inversion	SAMN00006366	Sequencing	Read depth and paired-end mapping	Homozygous	2,730
essv9921857	inversion	SAMN00006367	Sequencing	Read depth and paired-end mapping	Homozygous	2,481
essv9921858	inversion	SAMN00006368	Sequencing	Read depth and paired-end mapping	Homozygous	2,552

Showing 100 of 2240

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv9921759	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921760	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921761	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921762	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921763	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921764	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921765	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921766	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921767	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921768	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921769	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921770	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921771	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921772	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921773	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921774	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921775	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921776	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921777	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921778	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921779	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921780	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921781	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921782	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921783	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921784	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921785	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921786	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921787	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921788	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921789	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921790	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921791	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921792	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921793	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921794	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921795	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921796	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921797	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921798	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921799	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921800	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921801	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921802	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921803	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921804	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921805	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921806	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921807	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921808	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921809	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921810	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921811	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921812	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921813	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921814	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921815	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921816	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921817	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921818	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921819	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921820	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921821	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921822	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921823	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921824	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921825	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921826	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921827	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921828	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921829	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921830	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921831	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921832	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921833	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921834	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921835	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921836	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921837	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921838	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921839	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921840	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921841	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921842	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921843	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921844	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921845	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921846	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921847	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921848	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921849	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921850	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921851	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921852	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921853	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921854	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921855	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921856	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921857	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)
essv9921858	Remapped	Perfect	NC_000001.11:g.(43 593558_43593680)_( 43594218_43594340) inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	43,593,619 (-61, +61)	43,594,279 (-61, +61)

Showing 100 of 4480

dbVar

Database of genomic structural variation

esv3585870

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Variant Region Placement Information

Variant Call Information

Variant Call Placement Information

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.