esv3856296

Organism: Homo sapiens

Study:estd219 (1000 Genomes Consortium Phase 3 Integrated SV)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh37

Variant Calls:62
Validation:Not tested
Clinical Assertions: No
Region Size:18,880

Publication(s):1000 Genomes Consortium Phase 3 Integrated SV

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: 551 SVs from 62 studies. See in: genome view

Remapped(Score: Perfect):5,383,925-5,404,804

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3856296	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
esv3856296	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000009.11	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
essv21448858	deletion	HG00186	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,391
essv21448859	deletion	HG01242	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,454
essv21448860	deletion	HG01254	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	2,798
essv21448861	deletion	HG01518	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,132
essv21448862	deletion	HG01890	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,271
essv21448863	deletion	HG02143	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,045
essv21448864	deletion	HG02309	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,730
essv21448865	deletion	HG02325	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,782
essv21448866	deletion	HG02332	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,214
essv21448867	deletion	HG02455	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,875
essv21448868	deletion	HG02470	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,457
essv21448869	deletion	HG02554	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,307
essv21448870	deletion	HG02568	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,026
essv21448871	deletion	HG02583	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,904
essv21448872	deletion	HG02611	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,051
essv21448873	deletion	HG02620	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,179
essv21448874	deletion	HG02623	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,072
essv21448875	deletion	HG02629	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,928
essv21448876	deletion	HG02703	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,058
essv21448877	deletion	HG02716	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,025
essv21448878	deletion	HG02757	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,898
essv21448879	deletion	HG02759	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,148
essv21448880	deletion	HG02763	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,095
essv21448881	deletion	HG02768	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,980
essv21448882	deletion	HG02813	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,974
essv21448883	deletion	HG02814	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,874
essv21448884	deletion	HG02816	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,816
essv21448885	deletion	HG02878	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,249
essv21448886	deletion	HG02922	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,081
essv21448887	deletion	HG02941	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,309
essv21448888	deletion	HG03045	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,132
essv21448889	deletion	HG03046	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,832
essv21448890	deletion	HG03117	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,895
essv21448891	deletion	HG03130	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,940
essv21448892	deletion	HG03136	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,223
essv21448893	deletion	HG03313	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,432
essv21448894	deletion	HG03367	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,931
essv21448895	deletion	HG03442	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,030
essv21448896	deletion	HG03449	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,493
essv21448897	deletion	HG03470	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,775
essv21448898	deletion	HG03548	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,604
essv21448899	deletion	HG03558	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,190
essv21448900	deletion	HG03572	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,576
essv21448901	deletion	HG03583	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,621
essv21448902	deletion	NA18909	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,010
essv21448903	deletion	NA18916	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,991
essv21448904	deletion	NA18917	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,420
essv21448905	deletion	NA19019	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,959
essv21448906	deletion	NA19028	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,879
essv21448907	deletion	NA19095	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,949
essv21448908	deletion	NA19141	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,870
essv21448909	deletion	NA19213	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,956
essv21448910	deletion	NA19321	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,148
essv21448911	deletion	NA19377	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,671
essv21448912	deletion	NA19394	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,957
essv21448913	deletion	NA19439	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Homozygous	4,084
essv21448914	deletion	NA19448	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,637
essv21448915	deletion	NA19681	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,344
essv21448916	deletion	NA19788	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,263
essv21448917	deletion	NA20298	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,743
essv21448918	deletion	NA20508	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,447
essv21448919	deletion	NA20524	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,634

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv21448858	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448859	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448860	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448861	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448862	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448863	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448864	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448865	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448866	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448867	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448868	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448869	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448870	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448871	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448872	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448873	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448874	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448875	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448876	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448877	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448878	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448879	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448880	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448881	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448882	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448883	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448884	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448885	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448886	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448887	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448888	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448889	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448890	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448891	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448892	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448893	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448894	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448895	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448896	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448897	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448898	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448899	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448900	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448901	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448902	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448903	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448904	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448905	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448906	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448907	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448908	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448909	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448910	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448911	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448912	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448913	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448914	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448915	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448916	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448917	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448918	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448919	Remapped	Perfect	NC_000009.12:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448858	Submitted genomic		NC_000009.11:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh37 (hg19)		NC_000009.11	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448859	Submitted genomic		NC_000009.11:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh37 (hg19)		NC_000009.11	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448860	Submitted genomic		NC_000009.11:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh37 (hg19)		NC_000009.11	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448861	Submitted genomic		NC_000009.11:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh37 (hg19)		NC_000009.11	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448862	Submitted genomic		NC_000009.11:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh37 (hg19)		NC_000009.11	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448863	Submitted genomic		NC_000009.11:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh37 (hg19)		NC_000009.11	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448864	Submitted genomic		NC_000009.11:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh37 (hg19)		NC_000009.11	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448865	Submitted genomic		NC_000009.11:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh37 (hg19)		NC_000009.11	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448866	Submitted genomic		NC_000009.11:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh37 (hg19)		NC_000009.11	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448867	Submitted genomic		NC_000009.11:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh37 (hg19)		NC_000009.11	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448868	Submitted genomic		NC_000009.11:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh37 (hg19)		NC_000009.11	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448869	Submitted genomic		NC_000009.11:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh37 (hg19)		NC_000009.11	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448870	Submitted genomic		NC_000009.11:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh37 (hg19)		NC_000009.11	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448871	Submitted genomic		NC_000009.11:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh37 (hg19)		NC_000009.11	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448872	Submitted genomic		NC_000009.11:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh37 (hg19)		NC_000009.11	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448873	Submitted genomic		NC_000009.11:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh37 (hg19)		NC_000009.11	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448874	Submitted genomic		NC_000009.11:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh37 (hg19)		NC_000009.11	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448875	Submitted genomic		NC_000009.11:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh37 (hg19)		NC_000009.11	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448876	Submitted genomic		NC_000009.11:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh37 (hg19)		NC_000009.11	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448877	Submitted genomic		NC_000009.11:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh37 (hg19)		NC_000009.11	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448878	Submitted genomic		NC_000009.11:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh37 (hg19)		NC_000009.11	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448879	Submitted genomic		NC_000009.11:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh37 (hg19)		NC_000009.11	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448880	Submitted genomic		NC_000009.11:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh37 (hg19)		NC_000009.11	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448881	Submitted genomic		NC_000009.11:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh37 (hg19)		NC_000009.11	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448882	Submitted genomic		NC_000009.11:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh37 (hg19)		NC_000009.11	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448883	Submitted genomic		NC_000009.11:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh37 (hg19)		NC_000009.11	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448884	Submitted genomic		NC_000009.11:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh37 (hg19)		NC_000009.11	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448885	Submitted genomic		NC_000009.11:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh37 (hg19)		NC_000009.11	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448886	Submitted genomic		NC_000009.11:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh37 (hg19)		NC_000009.11	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448887	Submitted genomic		NC_000009.11:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh37 (hg19)		NC_000009.11	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448888	Submitted genomic		NC_000009.11:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh37 (hg19)		NC_000009.11	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448889	Submitted genomic		NC_000009.11:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh37 (hg19)		NC_000009.11	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448890	Submitted genomic		NC_000009.11:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh37 (hg19)		NC_000009.11	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448891	Submitted genomic		NC_000009.11:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh37 (hg19)		NC_000009.11	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448892	Submitted genomic		NC_000009.11:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh37 (hg19)		NC_000009.11	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448893	Submitted genomic		NC_000009.11:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh37 (hg19)		NC_000009.11	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448894	Submitted genomic		NC_000009.11:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh37 (hg19)		NC_000009.11	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)
essv21448895	Submitted genomic		NC_000009.11:g.(53 83925_5385425)_(54 03304_5404804)del	GRCh37 (hg19)		NC_000009.11	Chr9	5,384,925 (-1000, +500)	5,403,804 (-500, +1000)

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dbVar

Database of genomic structural variation

esv3856296

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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.