esv3641278

Organism: Homo sapiens

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

Variant Calls:39
Validation:Not tested
Clinical Assertions: No
Region Size:1,512

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: 156 SVs from 27 studies. See in: genome view

Remapped(Score: Perfect):76,181,660-76,183,283

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3641278	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000017.11	Chr17	76,181,716 (-56, +56)	76,183,227 (-56, +56)
esv3641278	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000017.10	Chr17	74,177,797 (-56, +56)	74,179,308 (-56, +56)

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
essv15742556	inversion	SAMN00016977	Sequencing	Read depth and paired-end mapping	Heterozygous	2,562
essv15742557	inversion	SAMN00006372	Sequencing	Read depth and paired-end mapping	Heterozygous	2,697
essv15742558	inversion	SAMN00009096	Sequencing	Read depth and paired-end mapping	Heterozygous	2,592
essv15742559	inversion	SAMN00006380	Sequencing	Read depth and paired-end mapping	Heterozygous	2,770
essv15742560	inversion	SAMN00006385	Sequencing	Read depth and paired-end mapping	Heterozygous	2,419
essv15742561	inversion	SAMN00006387	Sequencing	Read depth and paired-end mapping	Heterozygous	2,527
essv15742562	inversion	SAMN00006389	Sequencing	Read depth and paired-end mapping	Heterozygous	2,489
essv15742563	inversion	SAMN00009110	Sequencing	Read depth and paired-end mapping	Heterozygous	2,608
essv15742564	inversion	SAMN00006408	Sequencing	Read depth and paired-end mapping	Heterozygous	2,406
essv15742565	inversion	SAMN00006412	Sequencing	Read depth and paired-end mapping	Heterozygous	3,016
essv15742566	inversion	SAMN00006421	Sequencing	Read depth and paired-end mapping	Heterozygous	2,532
essv15742567	inversion	SAMN00006429	Sequencing	Read depth and paired-end mapping	Heterozygous	2,737
essv15742568	inversion	SAMN00009113	Sequencing	Read depth and paired-end mapping	Heterozygous	2,679
essv15742569	inversion	SAMN00006504	Sequencing	Read depth and paired-end mapping	Heterozygous	2,702
essv15742570	inversion	SAMN01091081	Sequencing	Read depth and paired-end mapping	Heterozygous	2,380
essv15742571	inversion	SAMN00009196	Sequencing	Read depth and paired-end mapping	Heterozygous	2,739
essv15742572	inversion	SAMN00014435	Sequencing	Read depth and paired-end mapping	Heterozygous	2,745
essv15742573	inversion	SAMN00016856	Sequencing	Read depth and paired-end mapping	Heterozygous	2,843
essv15742574	inversion	SAMN00249714	Sequencing	Read depth and paired-end mapping	Heterozygous	2,702
essv15742575	inversion	SAMN00630210	Sequencing	Read depth and paired-end mapping	Heterozygous	3,134
essv15742576	inversion	SAMN00263019	Sequencing	Read depth and paired-end mapping	Heterozygous	2,878
essv15742577	inversion	SAMN00263056	Sequencing	Read depth and paired-end mapping	Heterozygous	2,772
essv15742578	inversion	SAMN00630247	Sequencing	Read depth and paired-end mapping	Heterozygous	2,776
essv15742579	inversion	SAMN01761376	Sequencing	Read depth and paired-end mapping	Heterozygous	2,837
essv15742580	inversion	SAMN01096682	Sequencing	Read depth and paired-end mapping	Heterozygous	2,761
essv15742581	inversion	SAMN01090931	Sequencing	Read depth and paired-end mapping	Heterozygous	2,913
essv15742582	inversion	SAMN01090999	Sequencing	Read depth and paired-end mapping	Heterozygous	2,741
essv15742583	inversion	SAMN01761576	Sequencing	Read depth and paired-end mapping	Heterozygous	2,205
essv15742584	inversion	SAMN00797164	Sequencing	Read depth and paired-end mapping	Heterozygous	2,853
essv15742585	inversion	SAMN00800266	Sequencing	Read depth and paired-end mapping	Heterozygous	2,939
essv15742586	inversion	SAMN00800831	Sequencing	Read depth and paired-end mapping	Heterozygous	2,675
essv15742587	inversion	SAMN00801352	Sequencing	Read depth and paired-end mapping	Heterozygous	2,826
essv15742588	inversion	SAMN00801356	Sequencing	Read depth and paired-end mapping	Heterozygous	2,354
essv15742589	inversion	SAMN00110481	Sequencing	Read depth and paired-end mapping	Heterozygous	2,559
essv15742590	inversion	SAMN00007702	Sequencing	Read depth and paired-end mapping	Heterozygous	2,705
essv15742591	inversion	SAMN00001276	Sequencing	Read depth and paired-end mapping	Heterozygous	2,756
essv15742592	inversion	SAMN00004488	Sequencing	Read depth and paired-end mapping	Heterozygous	2,855
essv15742593	inversion	SAMN00007914	Sequencing	Read depth and paired-end mapping	Heterozygous	2,482
essv15742594	inversion	SAMN00007954	Sequencing	Read depth and paired-end mapping	Heterozygous	2,615

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv15742556	Remapped	Perfect	NC_000017.11:g.(76 181660_76181772)_( 76183171_76183283) inv	GRCh38.p12	First Pass	NC_000017.11	Chr17	76,181,716 (-56, +56)	76,183,227 (-56, +56)
essv15742557	Remapped	Perfect	NC_000017.11:g.(76 181660_76181772)_( 76183171_76183283) inv	GRCh38.p12	First Pass	NC_000017.11	Chr17	76,181,716 (-56, +56)	76,183,227 (-56, +56)
essv15742558	Remapped	Perfect	NC_000017.11:g.(76 181660_76181772)_( 76183171_76183283) inv	GRCh38.p12	First Pass	NC_000017.11	Chr17	76,181,716 (-56, +56)	76,183,227 (-56, +56)
essv15742559	Remapped	Perfect	NC_000017.11:g.(76 181660_76181772)_( 76183171_76183283) inv	GRCh38.p12	First Pass	NC_000017.11	Chr17	76,181,716 (-56, +56)	76,183,227 (-56, +56)
essv15742560	Remapped	Perfect	NC_000017.11:g.(76 181660_76181772)_( 76183171_76183283) inv	GRCh38.p12	First Pass	NC_000017.11	Chr17	76,181,716 (-56, +56)	76,183,227 (-56, +56)
essv15742561	Remapped	Perfect	NC_000017.11:g.(76 181660_76181772)_( 76183171_76183283) inv	GRCh38.p12	First Pass	NC_000017.11	Chr17	76,181,716 (-56, +56)	76,183,227 (-56, +56)
essv15742562	Remapped	Perfect	NC_000017.11:g.(76 181660_76181772)_( 76183171_76183283) inv	GRCh38.p12	First Pass	NC_000017.11	Chr17	76,181,716 (-56, +56)	76,183,227 (-56, +56)
essv15742563	Remapped	Perfect	NC_000017.11:g.(76 181660_76181772)_( 76183171_76183283) inv	GRCh38.p12	First Pass	NC_000017.11	Chr17	76,181,716 (-56, +56)	76,183,227 (-56, +56)
essv15742564	Remapped	Perfect	NC_000017.11:g.(76 181660_76181772)_( 76183171_76183283) inv	GRCh38.p12	First Pass	NC_000017.11	Chr17	76,181,716 (-56, +56)	76,183,227 (-56, +56)
essv15742565	Remapped	Perfect	NC_000017.11:g.(76 181660_76181772)_( 76183171_76183283) inv	GRCh38.p12	First Pass	NC_000017.11	Chr17	76,181,716 (-56, +56)	76,183,227 (-56, +56)
essv15742566	Remapped	Perfect	NC_000017.11:g.(76 181660_76181772)_( 76183171_76183283) inv	GRCh38.p12	First Pass	NC_000017.11	Chr17	76,181,716 (-56, +56)	76,183,227 (-56, +56)
essv15742567	Remapped	Perfect	NC_000017.11:g.(76 181660_76181772)_( 76183171_76183283) inv	GRCh38.p12	First Pass	NC_000017.11	Chr17	76,181,716 (-56, +56)	76,183,227 (-56, +56)
essv15742568	Remapped	Perfect	NC_000017.11:g.(76 181660_76181772)_( 76183171_76183283) inv	GRCh38.p12	First Pass	NC_000017.11	Chr17	76,181,716 (-56, +56)	76,183,227 (-56, +56)
essv15742569	Remapped	Perfect	NC_000017.11:g.(76 181660_76181772)_( 76183171_76183283) inv	GRCh38.p12	First Pass	NC_000017.11	Chr17	76,181,716 (-56, +56)	76,183,227 (-56, +56)
essv15742570	Remapped	Perfect	NC_000017.11:g.(76 181660_76181772)_( 76183171_76183283) inv	GRCh38.p12	First Pass	NC_000017.11	Chr17	76,181,716 (-56, +56)	76,183,227 (-56, +56)
essv15742571	Remapped	Perfect	NC_000017.11:g.(76 181660_76181772)_( 76183171_76183283) inv	GRCh38.p12	First Pass	NC_000017.11	Chr17	76,181,716 (-56, +56)	76,183,227 (-56, +56)
essv15742572	Remapped	Perfect	NC_000017.11:g.(76 181660_76181772)_( 76183171_76183283) inv	GRCh38.p12	First Pass	NC_000017.11	Chr17	76,181,716 (-56, +56)	76,183,227 (-56, +56)
essv15742573	Remapped	Perfect	NC_000017.11:g.(76 181660_76181772)_( 76183171_76183283) inv	GRCh38.p12	First Pass	NC_000017.11	Chr17	76,181,716 (-56, +56)	76,183,227 (-56, +56)
essv15742574	Remapped	Perfect	NC_000017.11:g.(76 181660_76181772)_( 76183171_76183283) inv	GRCh38.p12	First Pass	NC_000017.11	Chr17	76,181,716 (-56, +56)	76,183,227 (-56, +56)
essv15742575	Remapped	Perfect	NC_000017.11:g.(76 181660_76181772)_( 76183171_76183283) inv	GRCh38.p12	First Pass	NC_000017.11	Chr17	76,181,716 (-56, +56)	76,183,227 (-56, +56)
essv15742576	Remapped	Perfect	NC_000017.11:g.(76 181660_76181772)_( 76183171_76183283) inv	GRCh38.p12	First Pass	NC_000017.11	Chr17	76,181,716 (-56, +56)	76,183,227 (-56, +56)
essv15742577	Remapped	Perfect	NC_000017.11:g.(76 181660_76181772)_( 76183171_76183283) inv	GRCh38.p12	First Pass	NC_000017.11	Chr17	76,181,716 (-56, +56)	76,183,227 (-56, +56)
essv15742578	Remapped	Perfect	NC_000017.11:g.(76 181660_76181772)_( 76183171_76183283) inv	GRCh38.p12	First Pass	NC_000017.11	Chr17	76,181,716 (-56, +56)	76,183,227 (-56, +56)
essv15742579	Remapped	Perfect	NC_000017.11:g.(76 181660_76181772)_( 76183171_76183283) inv	GRCh38.p12	First Pass	NC_000017.11	Chr17	76,181,716 (-56, +56)	76,183,227 (-56, +56)
essv15742580	Remapped	Perfect	NC_000017.11:g.(76 181660_76181772)_( 76183171_76183283) inv	GRCh38.p12	First Pass	NC_000017.11	Chr17	76,181,716 (-56, +56)	76,183,227 (-56, +56)
essv15742581	Remapped	Perfect	NC_000017.11:g.(76 181660_76181772)_( 76183171_76183283) inv	GRCh38.p12	First Pass	NC_000017.11	Chr17	76,181,716 (-56, +56)	76,183,227 (-56, +56)
essv15742582	Remapped	Perfect	NC_000017.11:g.(76 181660_76181772)_( 76183171_76183283) inv	GRCh38.p12	First Pass	NC_000017.11	Chr17	76,181,716 (-56, +56)	76,183,227 (-56, +56)
essv15742583	Remapped	Perfect	NC_000017.11:g.(76 181660_76181772)_( 76183171_76183283) inv	GRCh38.p12	First Pass	NC_000017.11	Chr17	76,181,716 (-56, +56)	76,183,227 (-56, +56)
essv15742584	Remapped	Perfect	NC_000017.11:g.(76 181660_76181772)_( 76183171_76183283) inv	GRCh38.p12	First Pass	NC_000017.11	Chr17	76,181,716 (-56, +56)	76,183,227 (-56, +56)
essv15742585	Remapped	Perfect	NC_000017.11:g.(76 181660_76181772)_( 76183171_76183283) inv	GRCh38.p12	First Pass	NC_000017.11	Chr17	76,181,716 (-56, +56)	76,183,227 (-56, +56)
essv15742586	Remapped	Perfect	NC_000017.11:g.(76 181660_76181772)_( 76183171_76183283) inv	GRCh38.p12	First Pass	NC_000017.11	Chr17	76,181,716 (-56, +56)	76,183,227 (-56, +56)
essv15742587	Remapped	Perfect	NC_000017.11:g.(76 181660_76181772)_( 76183171_76183283) inv	GRCh38.p12	First Pass	NC_000017.11	Chr17	76,181,716 (-56, +56)	76,183,227 (-56, +56)
essv15742588	Remapped	Perfect	NC_000017.11:g.(76 181660_76181772)_( 76183171_76183283) inv	GRCh38.p12	First Pass	NC_000017.11	Chr17	76,181,716 (-56, +56)	76,183,227 (-56, +56)
essv15742589	Remapped	Perfect	NC_000017.11:g.(76 181660_76181772)_( 76183171_76183283) inv	GRCh38.p12	First Pass	NC_000017.11	Chr17	76,181,716 (-56, +56)	76,183,227 (-56, +56)
essv15742590	Remapped	Perfect	NC_000017.11:g.(76 181660_76181772)_( 76183171_76183283) inv	GRCh38.p12	First Pass	NC_000017.11	Chr17	76,181,716 (-56, +56)	76,183,227 (-56, +56)
essv15742591	Remapped	Perfect	NC_000017.11:g.(76 181660_76181772)_( 76183171_76183283) inv	GRCh38.p12	First Pass	NC_000017.11	Chr17	76,181,716 (-56, +56)	76,183,227 (-56, +56)
essv15742592	Remapped	Perfect	NC_000017.11:g.(76 181660_76181772)_( 76183171_76183283) inv	GRCh38.p12	First Pass	NC_000017.11	Chr17	76,181,716 (-56, +56)	76,183,227 (-56, +56)
essv15742593	Remapped	Perfect	NC_000017.11:g.(76 181660_76181772)_( 76183171_76183283) inv	GRCh38.p12	First Pass	NC_000017.11	Chr17	76,181,716 (-56, +56)	76,183,227 (-56, +56)
essv15742594	Remapped	Perfect	NC_000017.11:g.(76 181660_76181772)_( 76183171_76183283) inv	GRCh38.p12	First Pass	NC_000017.11	Chr17	76,181,716 (-56, +56)	76,183,227 (-56, +56)
essv15742556	Submitted genomic		NC_000017.10:g.(74 177741_74177853)_( 74179252_74179364) inv	GRCh37 (hg19)		NC_000017.10	Chr17	74,177,797 (-56, +56)	74,179,308 (-56, +56)
essv15742557	Submitted genomic		NC_000017.10:g.(74 177741_74177853)_( 74179252_74179364) inv	GRCh37 (hg19)		NC_000017.10	Chr17	74,177,797 (-56, +56)	74,179,308 (-56, +56)
essv15742558	Submitted genomic		NC_000017.10:g.(74 177741_74177853)_( 74179252_74179364) inv	GRCh37 (hg19)		NC_000017.10	Chr17	74,177,797 (-56, +56)	74,179,308 (-56, +56)
essv15742559	Submitted genomic		NC_000017.10:g.(74 177741_74177853)_( 74179252_74179364) inv	GRCh37 (hg19)		NC_000017.10	Chr17	74,177,797 (-56, +56)	74,179,308 (-56, +56)
essv15742560	Submitted genomic		NC_000017.10:g.(74 177741_74177853)_( 74179252_74179364) inv	GRCh37 (hg19)		NC_000017.10	Chr17	74,177,797 (-56, +56)	74,179,308 (-56, +56)
essv15742561	Submitted genomic		NC_000017.10:g.(74 177741_74177853)_( 74179252_74179364) inv	GRCh37 (hg19)		NC_000017.10	Chr17	74,177,797 (-56, +56)	74,179,308 (-56, +56)
essv15742562	Submitted genomic		NC_000017.10:g.(74 177741_74177853)_( 74179252_74179364) inv	GRCh37 (hg19)		NC_000017.10	Chr17	74,177,797 (-56, +56)	74,179,308 (-56, +56)
essv15742563	Submitted genomic		NC_000017.10:g.(74 177741_74177853)_( 74179252_74179364) inv	GRCh37 (hg19)		NC_000017.10	Chr17	74,177,797 (-56, +56)	74,179,308 (-56, +56)
essv15742564	Submitted genomic		NC_000017.10:g.(74 177741_74177853)_( 74179252_74179364) inv	GRCh37 (hg19)		NC_000017.10	Chr17	74,177,797 (-56, +56)	74,179,308 (-56, +56)
essv15742565	Submitted genomic		NC_000017.10:g.(74 177741_74177853)_( 74179252_74179364) inv	GRCh37 (hg19)		NC_000017.10	Chr17	74,177,797 (-56, +56)	74,179,308 (-56, +56)
essv15742566	Submitted genomic		NC_000017.10:g.(74 177741_74177853)_( 74179252_74179364) inv	GRCh37 (hg19)		NC_000017.10	Chr17	74,177,797 (-56, +56)	74,179,308 (-56, +56)
essv15742567	Submitted genomic		NC_000017.10:g.(74 177741_74177853)_( 74179252_74179364) inv	GRCh37 (hg19)		NC_000017.10	Chr17	74,177,797 (-56, +56)	74,179,308 (-56, +56)
essv15742568	Submitted genomic		NC_000017.10:g.(74 177741_74177853)_( 74179252_74179364) inv	GRCh37 (hg19)		NC_000017.10	Chr17	74,177,797 (-56, +56)	74,179,308 (-56, +56)
essv15742569	Submitted genomic		NC_000017.10:g.(74 177741_74177853)_( 74179252_74179364) inv	GRCh37 (hg19)		NC_000017.10	Chr17	74,177,797 (-56, +56)	74,179,308 (-56, +56)
essv15742570	Submitted genomic		NC_000017.10:g.(74 177741_74177853)_( 74179252_74179364) inv	GRCh37 (hg19)		NC_000017.10	Chr17	74,177,797 (-56, +56)	74,179,308 (-56, +56)
essv15742571	Submitted genomic		NC_000017.10:g.(74 177741_74177853)_( 74179252_74179364) inv	GRCh37 (hg19)		NC_000017.10	Chr17	74,177,797 (-56, +56)	74,179,308 (-56, +56)
essv15742572	Submitted genomic		NC_000017.10:g.(74 177741_74177853)_( 74179252_74179364) inv	GRCh37 (hg19)		NC_000017.10	Chr17	74,177,797 (-56, +56)	74,179,308 (-56, +56)
essv15742573	Submitted genomic		NC_000017.10:g.(74 177741_74177853)_( 74179252_74179364) inv	GRCh37 (hg19)		NC_000017.10	Chr17	74,177,797 (-56, +56)	74,179,308 (-56, +56)
essv15742574	Submitted genomic		NC_000017.10:g.(74 177741_74177853)_( 74179252_74179364) inv	GRCh37 (hg19)		NC_000017.10	Chr17	74,177,797 (-56, +56)	74,179,308 (-56, +56)
essv15742575	Submitted genomic		NC_000017.10:g.(74 177741_74177853)_( 74179252_74179364) inv	GRCh37 (hg19)		NC_000017.10	Chr17	74,177,797 (-56, +56)	74,179,308 (-56, +56)
essv15742576	Submitted genomic		NC_000017.10:g.(74 177741_74177853)_( 74179252_74179364) inv	GRCh37 (hg19)		NC_000017.10	Chr17	74,177,797 (-56, +56)	74,179,308 (-56, +56)
essv15742577	Submitted genomic		NC_000017.10:g.(74 177741_74177853)_( 74179252_74179364) inv	GRCh37 (hg19)		NC_000017.10	Chr17	74,177,797 (-56, +56)	74,179,308 (-56, +56)
essv15742578	Submitted genomic		NC_000017.10:g.(74 177741_74177853)_( 74179252_74179364) inv	GRCh37 (hg19)		NC_000017.10	Chr17	74,177,797 (-56, +56)	74,179,308 (-56, +56)
essv15742579	Submitted genomic		NC_000017.10:g.(74 177741_74177853)_( 74179252_74179364) inv	GRCh37 (hg19)		NC_000017.10	Chr17	74,177,797 (-56, +56)	74,179,308 (-56, +56)
essv15742580	Submitted genomic		NC_000017.10:g.(74 177741_74177853)_( 74179252_74179364) inv	GRCh37 (hg19)		NC_000017.10	Chr17	74,177,797 (-56, +56)	74,179,308 (-56, +56)
essv15742581	Submitted genomic		NC_000017.10:g.(74 177741_74177853)_( 74179252_74179364) inv	GRCh37 (hg19)		NC_000017.10	Chr17	74,177,797 (-56, +56)	74,179,308 (-56, +56)
essv15742582	Submitted genomic		NC_000017.10:g.(74 177741_74177853)_( 74179252_74179364) inv	GRCh37 (hg19)		NC_000017.10	Chr17	74,177,797 (-56, +56)	74,179,308 (-56, +56)
essv15742583	Submitted genomic		NC_000017.10:g.(74 177741_74177853)_( 74179252_74179364) inv	GRCh37 (hg19)		NC_000017.10	Chr17	74,177,797 (-56, +56)	74,179,308 (-56, +56)
essv15742584	Submitted genomic		NC_000017.10:g.(74 177741_74177853)_( 74179252_74179364) inv	GRCh37 (hg19)		NC_000017.10	Chr17	74,177,797 (-56, +56)	74,179,308 (-56, +56)
essv15742585	Submitted genomic		NC_000017.10:g.(74 177741_74177853)_( 74179252_74179364) inv	GRCh37 (hg19)		NC_000017.10	Chr17	74,177,797 (-56, +56)	74,179,308 (-56, +56)
essv15742586	Submitted genomic		NC_000017.10:g.(74 177741_74177853)_( 74179252_74179364) inv	GRCh37 (hg19)		NC_000017.10	Chr17	74,177,797 (-56, +56)	74,179,308 (-56, +56)
essv15742587	Submitted genomic		NC_000017.10:g.(74 177741_74177853)_( 74179252_74179364) inv	GRCh37 (hg19)		NC_000017.10	Chr17	74,177,797 (-56, +56)	74,179,308 (-56, +56)
essv15742588	Submitted genomic		NC_000017.10:g.(74 177741_74177853)_( 74179252_74179364) inv	GRCh37 (hg19)		NC_000017.10	Chr17	74,177,797 (-56, +56)	74,179,308 (-56, +56)
essv15742589	Submitted genomic		NC_000017.10:g.(74 177741_74177853)_( 74179252_74179364) inv	GRCh37 (hg19)		NC_000017.10	Chr17	74,177,797 (-56, +56)	74,179,308 (-56, +56)
essv15742590	Submitted genomic		NC_000017.10:g.(74 177741_74177853)_( 74179252_74179364) inv	GRCh37 (hg19)		NC_000017.10	Chr17	74,177,797 (-56, +56)	74,179,308 (-56, +56)
essv15742591	Submitted genomic		NC_000017.10:g.(74 177741_74177853)_( 74179252_74179364) inv	GRCh37 (hg19)		NC_000017.10	Chr17	74,177,797 (-56, +56)	74,179,308 (-56, +56)
essv15742592	Submitted genomic		NC_000017.10:g.(74 177741_74177853)_( 74179252_74179364) inv	GRCh37 (hg19)		NC_000017.10	Chr17	74,177,797 (-56, +56)	74,179,308 (-56, +56)
essv15742593	Submitted genomic		NC_000017.10:g.(74 177741_74177853)_( 74179252_74179364) inv	GRCh37 (hg19)		NC_000017.10	Chr17	74,177,797 (-56, +56)	74,179,308 (-56, +56)
essv15742594	Submitted genomic		NC_000017.10:g.(74 177741_74177853)_( 74179252_74179364) inv	GRCh37 (hg19)		NC_000017.10	Chr17	74,177,797 (-56, +56)	74,179,308 (-56, +56)

dbVar

Database of genomic structural variation

esv3641278

Links to Other Resources

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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.