esv3632019

Organism: Homo sapiens

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

Variant Calls:41
Validation:Not tested
Clinical Assertions: No
Region Size:7,378

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: 244 SVs from 38 studies. See in: genome view

Remapped(Score: Perfect):48,199,030-48,206,829

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3632019	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000013.11	Chr13	48,199,241 (-211, +211)	48,206,618 (-211, +211)
esv3632019	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000013.10	Chr13	48,773,377 (-211, +211)	48,780,754 (-211, +211)

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
essv14716014	inversion	SAMN00630200	Sequencing	Read depth and paired-end mapping	Heterozygous	3,059
essv14716015	inversion	SAMN00255127	Sequencing	Read depth and paired-end mapping	Heterozygous	3,380
essv14716016	inversion	SAMN00630212	Sequencing	Read depth and paired-end mapping	Heterozygous	3,142
essv14716017	inversion	SAMN00262986	Sequencing	Read depth and paired-end mapping	Heterozygous	3,389
essv14716018	inversion	SAMN00630219	Sequencing	Read depth and paired-end mapping	Heterozygous	3,239
essv14716019	inversion	SAMN00630222	Sequencing	Read depth and paired-end mapping	Heterozygous	3,114
essv14716020	inversion	SAMN00630223	Sequencing	Read depth and paired-end mapping	Heterozygous	3,177
essv14716021	inversion	SAMN00630238	Sequencing	Read depth and paired-end mapping	Heterozygous	2,511
essv14716022	inversion	SAMN01091043	Sequencing	Read depth and paired-end mapping	Heterozygous	2,937
essv14716023	inversion	SAMN01091048	Sequencing	Read depth and paired-end mapping	Heterozygous	2,346
essv14716024	inversion	SAMN00779976	Sequencing	Read depth and paired-end mapping	Heterozygous	3,129
essv14716025	inversion	SAMN00779982	Sequencing	Read depth and paired-end mapping	Heterozygous	3,199
essv14716026	inversion	SAMN01036716	Sequencing	Read depth and paired-end mapping	Heterozygous	3,159
essv14716027	inversion	SAMN01036725	Sequencing	Read depth and paired-end mapping	Heterozygous	3,135
essv14716028	inversion	SAMN01036776	Sequencing	Read depth and paired-end mapping	Heterozygous	2,914
essv14716029	inversion	SAMN01036795	Sequencing	Read depth and paired-end mapping	Homozygous	3,333
essv14716030	inversion	SAMN01036797	Sequencing	Read depth and paired-end mapping	Heterozygous	3,180
essv14716031	inversion	SAMN01090864	Sequencing	Read depth and paired-end mapping	Heterozygous	2,852
essv14716032	inversion	SAMN01036810	Sequencing	Read depth and paired-end mapping	Heterozygous	3,221
essv14716033	inversion	SAMN01090874	Sequencing	Read depth and paired-end mapping	Heterozygous	3,163
essv14716034	inversion	SAMN01090877	Sequencing	Read depth and paired-end mapping	Heterozygous	3,074
essv14716035	inversion	SAMN01090901	Sequencing	Read depth and paired-end mapping	Homozygous	3,003
essv14716036	inversion	SAMN01090818	Sequencing	Read depth and paired-end mapping	Heterozygous	3,288
essv14716037	inversion	SAMN01090792	Sequencing	Read depth and paired-end mapping	Heterozygous	3,179
essv14716038	inversion	SAMN01036793	Sequencing	Read depth and paired-end mapping	Heterozygous	3,204
essv14716039	inversion	SAMN01090793	Sequencing	Read depth and paired-end mapping	Heterozygous	2,951
essv14716040	inversion	SAMN01090811	Sequencing	Read depth and paired-end mapping	Heterozygous	3,042
essv14716041	inversion	SAMN01761353	Sequencing	Read depth and paired-end mapping	Homozygous	3,438
essv14716042	inversion	SAMN00001583	Sequencing	Read depth and paired-end mapping	Heterozygous	3,337
essv14716043	inversion	SAMN00001019	Sequencing	Read depth and paired-end mapping	Heterozygous	3,288
essv14716044	inversion	SAMN00001631	Sequencing	Read depth and paired-end mapping	Heterozygous	3,116
essv14716045	inversion	SAMN00000552	Sequencing	Read depth and paired-end mapping	Heterozygous	2,797
essv14716046	inversion	SAMN00001670	Sequencing	Read depth and paired-end mapping	Heterozygous	3,144
essv14716047	inversion	SAMN00001674	Sequencing	Read depth and paired-end mapping	Heterozygous	3,102
essv14716048	inversion	SAMN00000565	Sequencing	Read depth and paired-end mapping	Heterozygous	3,208
essv14716049	inversion	SAMN00001115	Sequencing	Read depth and paired-end mapping	Heterozygous	2,431
essv14716050	inversion	SAMN00001152	Sequencing	Read depth and paired-end mapping	Heterozygous	3,097
essv14716051	inversion	SAMN00001160	Sequencing	Read depth and paired-end mapping	Heterozygous	2,641
essv14716052	inversion	SAMN00007830	Sequencing	Read depth and paired-end mapping	Heterozygous	2,530
essv14716053	inversion	SAMN00007841	Sequencing	Read depth and paired-end mapping	Heterozygous	2,528
essv14716054	inversion	SAMN00007862	Sequencing	Read depth and paired-end mapping	Heterozygous	2,399

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv14716014	Remapped	Perfect	NC_000013.11:g.(48 199030_48199452)_( 48206407_48206829) inv	GRCh38.p12	First Pass	NC_000013.11	Chr13	48,199,241 (-211, +211)	48,206,618 (-211, +211)
essv14716015	Remapped	Perfect	NC_000013.11:g.(48 199030_48199452)_( 48206407_48206829) inv	GRCh38.p12	First Pass	NC_000013.11	Chr13	48,199,241 (-211, +211)	48,206,618 (-211, +211)
essv14716016	Remapped	Perfect	NC_000013.11:g.(48 199030_48199452)_( 48206407_48206829) inv	GRCh38.p12	First Pass	NC_000013.11	Chr13	48,199,241 (-211, +211)	48,206,618 (-211, +211)
essv14716017	Remapped	Perfect	NC_000013.11:g.(48 199030_48199452)_( 48206407_48206829) inv	GRCh38.p12	First Pass	NC_000013.11	Chr13	48,199,241 (-211, +211)	48,206,618 (-211, +211)
essv14716018	Remapped	Perfect	NC_000013.11:g.(48 199030_48199452)_( 48206407_48206829) inv	GRCh38.p12	First Pass	NC_000013.11	Chr13	48,199,241 (-211, +211)	48,206,618 (-211, +211)
essv14716019	Remapped	Perfect	NC_000013.11:g.(48 199030_48199452)_( 48206407_48206829) inv	GRCh38.p12	First Pass	NC_000013.11	Chr13	48,199,241 (-211, +211)	48,206,618 (-211, +211)
essv14716020	Remapped	Perfect	NC_000013.11:g.(48 199030_48199452)_( 48206407_48206829) inv	GRCh38.p12	First Pass	NC_000013.11	Chr13	48,199,241 (-211, +211)	48,206,618 (-211, +211)
essv14716021	Remapped	Perfect	NC_000013.11:g.(48 199030_48199452)_( 48206407_48206829) inv	GRCh38.p12	First Pass	NC_000013.11	Chr13	48,199,241 (-211, +211)	48,206,618 (-211, +211)
essv14716022	Remapped	Perfect	NC_000013.11:g.(48 199030_48199452)_( 48206407_48206829) inv	GRCh38.p12	First Pass	NC_000013.11	Chr13	48,199,241 (-211, +211)	48,206,618 (-211, +211)
essv14716023	Remapped	Perfect	NC_000013.11:g.(48 199030_48199452)_( 48206407_48206829) inv	GRCh38.p12	First Pass	NC_000013.11	Chr13	48,199,241 (-211, +211)	48,206,618 (-211, +211)
essv14716024	Remapped	Perfect	NC_000013.11:g.(48 199030_48199452)_( 48206407_48206829) inv	GRCh38.p12	First Pass	NC_000013.11	Chr13	48,199,241 (-211, +211)	48,206,618 (-211, +211)
essv14716025	Remapped	Perfect	NC_000013.11:g.(48 199030_48199452)_( 48206407_48206829) inv	GRCh38.p12	First Pass	NC_000013.11	Chr13	48,199,241 (-211, +211)	48,206,618 (-211, +211)
essv14716026	Remapped	Perfect	NC_000013.11:g.(48 199030_48199452)_( 48206407_48206829) inv	GRCh38.p12	First Pass	NC_000013.11	Chr13	48,199,241 (-211, +211)	48,206,618 (-211, +211)
essv14716027	Remapped	Perfect	NC_000013.11:g.(48 199030_48199452)_( 48206407_48206829) inv	GRCh38.p12	First Pass	NC_000013.11	Chr13	48,199,241 (-211, +211)	48,206,618 (-211, +211)
essv14716028	Remapped	Perfect	NC_000013.11:g.(48 199030_48199452)_( 48206407_48206829) inv	GRCh38.p12	First Pass	NC_000013.11	Chr13	48,199,241 (-211, +211)	48,206,618 (-211, +211)
essv14716029	Remapped	Perfect	NC_000013.11:g.(48 199030_48199452)_( 48206407_48206829) inv	GRCh38.p12	First Pass	NC_000013.11	Chr13	48,199,241 (-211, +211)	48,206,618 (-211, +211)
essv14716030	Remapped	Perfect	NC_000013.11:g.(48 199030_48199452)_( 48206407_48206829) inv	GRCh38.p12	First Pass	NC_000013.11	Chr13	48,199,241 (-211, +211)	48,206,618 (-211, +211)
essv14716031	Remapped	Perfect	NC_000013.11:g.(48 199030_48199452)_( 48206407_48206829) inv	GRCh38.p12	First Pass	NC_000013.11	Chr13	48,199,241 (-211, +211)	48,206,618 (-211, +211)
essv14716032	Remapped	Perfect	NC_000013.11:g.(48 199030_48199452)_( 48206407_48206829) inv	GRCh38.p12	First Pass	NC_000013.11	Chr13	48,199,241 (-211, +211)	48,206,618 (-211, +211)
essv14716033	Remapped	Perfect	NC_000013.11:g.(48 199030_48199452)_( 48206407_48206829) inv	GRCh38.p12	First Pass	NC_000013.11	Chr13	48,199,241 (-211, +211)	48,206,618 (-211, +211)
essv14716034	Remapped	Perfect	NC_000013.11:g.(48 199030_48199452)_( 48206407_48206829) inv	GRCh38.p12	First Pass	NC_000013.11	Chr13	48,199,241 (-211, +211)	48,206,618 (-211, +211)
essv14716035	Remapped	Perfect	NC_000013.11:g.(48 199030_48199452)_( 48206407_48206829) inv	GRCh38.p12	First Pass	NC_000013.11	Chr13	48,199,241 (-211, +211)	48,206,618 (-211, +211)
essv14716036	Remapped	Perfect	NC_000013.11:g.(48 199030_48199452)_( 48206407_48206829) inv	GRCh38.p12	First Pass	NC_000013.11	Chr13	48,199,241 (-211, +211)	48,206,618 (-211, +211)
essv14716037	Remapped	Perfect	NC_000013.11:g.(48 199030_48199452)_( 48206407_48206829) inv	GRCh38.p12	First Pass	NC_000013.11	Chr13	48,199,241 (-211, +211)	48,206,618 (-211, +211)
essv14716038	Remapped	Perfect	NC_000013.11:g.(48 199030_48199452)_( 48206407_48206829) inv	GRCh38.p12	First Pass	NC_000013.11	Chr13	48,199,241 (-211, +211)	48,206,618 (-211, +211)
essv14716039	Remapped	Perfect	NC_000013.11:g.(48 199030_48199452)_( 48206407_48206829) inv	GRCh38.p12	First Pass	NC_000013.11	Chr13	48,199,241 (-211, +211)	48,206,618 (-211, +211)
essv14716040	Remapped	Perfect	NC_000013.11:g.(48 199030_48199452)_( 48206407_48206829) inv	GRCh38.p12	First Pass	NC_000013.11	Chr13	48,199,241 (-211, +211)	48,206,618 (-211, +211)
essv14716041	Remapped	Perfect	NC_000013.11:g.(48 199030_48199452)_( 48206407_48206829) inv	GRCh38.p12	First Pass	NC_000013.11	Chr13	48,199,241 (-211, +211)	48,206,618 (-211, +211)
essv14716042	Remapped	Perfect	NC_000013.11:g.(48 199030_48199452)_( 48206407_48206829) inv	GRCh38.p12	First Pass	NC_000013.11	Chr13	48,199,241 (-211, +211)	48,206,618 (-211, +211)
essv14716043	Remapped	Perfect	NC_000013.11:g.(48 199030_48199452)_( 48206407_48206829) inv	GRCh38.p12	First Pass	NC_000013.11	Chr13	48,199,241 (-211, +211)	48,206,618 (-211, +211)
essv14716044	Remapped	Perfect	NC_000013.11:g.(48 199030_48199452)_( 48206407_48206829) inv	GRCh38.p12	First Pass	NC_000013.11	Chr13	48,199,241 (-211, +211)	48,206,618 (-211, +211)
essv14716045	Remapped	Perfect	NC_000013.11:g.(48 199030_48199452)_( 48206407_48206829) inv	GRCh38.p12	First Pass	NC_000013.11	Chr13	48,199,241 (-211, +211)	48,206,618 (-211, +211)
essv14716046	Remapped	Perfect	NC_000013.11:g.(48 199030_48199452)_( 48206407_48206829) inv	GRCh38.p12	First Pass	NC_000013.11	Chr13	48,199,241 (-211, +211)	48,206,618 (-211, +211)
essv14716047	Remapped	Perfect	NC_000013.11:g.(48 199030_48199452)_( 48206407_48206829) inv	GRCh38.p12	First Pass	NC_000013.11	Chr13	48,199,241 (-211, +211)	48,206,618 (-211, +211)
essv14716048	Remapped	Perfect	NC_000013.11:g.(48 199030_48199452)_( 48206407_48206829) inv	GRCh38.p12	First Pass	NC_000013.11	Chr13	48,199,241 (-211, +211)	48,206,618 (-211, +211)
essv14716049	Remapped	Perfect	NC_000013.11:g.(48 199030_48199452)_( 48206407_48206829) inv	GRCh38.p12	First Pass	NC_000013.11	Chr13	48,199,241 (-211, +211)	48,206,618 (-211, +211)
essv14716050	Remapped	Perfect	NC_000013.11:g.(48 199030_48199452)_( 48206407_48206829) inv	GRCh38.p12	First Pass	NC_000013.11	Chr13	48,199,241 (-211, +211)	48,206,618 (-211, +211)
essv14716051	Remapped	Perfect	NC_000013.11:g.(48 199030_48199452)_( 48206407_48206829) inv	GRCh38.p12	First Pass	NC_000013.11	Chr13	48,199,241 (-211, +211)	48,206,618 (-211, +211)
essv14716052	Remapped	Perfect	NC_000013.11:g.(48 199030_48199452)_( 48206407_48206829) inv	GRCh38.p12	First Pass	NC_000013.11	Chr13	48,199,241 (-211, +211)	48,206,618 (-211, +211)
essv14716053	Remapped	Perfect	NC_000013.11:g.(48 199030_48199452)_( 48206407_48206829) inv	GRCh38.p12	First Pass	NC_000013.11	Chr13	48,199,241 (-211, +211)	48,206,618 (-211, +211)
essv14716054	Remapped	Perfect	NC_000013.11:g.(48 199030_48199452)_( 48206407_48206829) inv	GRCh38.p12	First Pass	NC_000013.11	Chr13	48,199,241 (-211, +211)	48,206,618 (-211, +211)
essv14716014	Submitted genomic		NC_000013.10:g.(48 773166_48773588)_( 48780543_48780965) inv	GRCh37 (hg19)		NC_000013.10	Chr13	48,773,377 (-211, +211)	48,780,754 (-211, +211)
essv14716015	Submitted genomic		NC_000013.10:g.(48 773166_48773588)_( 48780543_48780965) inv	GRCh37 (hg19)		NC_000013.10	Chr13	48,773,377 (-211, +211)	48,780,754 (-211, +211)
essv14716016	Submitted genomic		NC_000013.10:g.(48 773166_48773588)_( 48780543_48780965) inv	GRCh37 (hg19)		NC_000013.10	Chr13	48,773,377 (-211, +211)	48,780,754 (-211, +211)
essv14716017	Submitted genomic		NC_000013.10:g.(48 773166_48773588)_( 48780543_48780965) inv	GRCh37 (hg19)		NC_000013.10	Chr13	48,773,377 (-211, +211)	48,780,754 (-211, +211)
essv14716018	Submitted genomic		NC_000013.10:g.(48 773166_48773588)_( 48780543_48780965) inv	GRCh37 (hg19)		NC_000013.10	Chr13	48,773,377 (-211, +211)	48,780,754 (-211, +211)
essv14716019	Submitted genomic		NC_000013.10:g.(48 773166_48773588)_( 48780543_48780965) inv	GRCh37 (hg19)		NC_000013.10	Chr13	48,773,377 (-211, +211)	48,780,754 (-211, +211)
essv14716020	Submitted genomic		NC_000013.10:g.(48 773166_48773588)_( 48780543_48780965) inv	GRCh37 (hg19)		NC_000013.10	Chr13	48,773,377 (-211, +211)	48,780,754 (-211, +211)
essv14716021	Submitted genomic		NC_000013.10:g.(48 773166_48773588)_( 48780543_48780965) inv	GRCh37 (hg19)		NC_000013.10	Chr13	48,773,377 (-211, +211)	48,780,754 (-211, +211)
essv14716022	Submitted genomic		NC_000013.10:g.(48 773166_48773588)_( 48780543_48780965) inv	GRCh37 (hg19)		NC_000013.10	Chr13	48,773,377 (-211, +211)	48,780,754 (-211, +211)
essv14716023	Submitted genomic		NC_000013.10:g.(48 773166_48773588)_( 48780543_48780965) inv	GRCh37 (hg19)		NC_000013.10	Chr13	48,773,377 (-211, +211)	48,780,754 (-211, +211)
essv14716024	Submitted genomic		NC_000013.10:g.(48 773166_48773588)_( 48780543_48780965) inv	GRCh37 (hg19)		NC_000013.10	Chr13	48,773,377 (-211, +211)	48,780,754 (-211, +211)
essv14716025	Submitted genomic		NC_000013.10:g.(48 773166_48773588)_( 48780543_48780965) inv	GRCh37 (hg19)		NC_000013.10	Chr13	48,773,377 (-211, +211)	48,780,754 (-211, +211)
essv14716026	Submitted genomic		NC_000013.10:g.(48 773166_48773588)_( 48780543_48780965) inv	GRCh37 (hg19)		NC_000013.10	Chr13	48,773,377 (-211, +211)	48,780,754 (-211, +211)
essv14716027	Submitted genomic		NC_000013.10:g.(48 773166_48773588)_( 48780543_48780965) inv	GRCh37 (hg19)		NC_000013.10	Chr13	48,773,377 (-211, +211)	48,780,754 (-211, +211)
essv14716028	Submitted genomic		NC_000013.10:g.(48 773166_48773588)_( 48780543_48780965) inv	GRCh37 (hg19)		NC_000013.10	Chr13	48,773,377 (-211, +211)	48,780,754 (-211, +211)
essv14716029	Submitted genomic		NC_000013.10:g.(48 773166_48773588)_( 48780543_48780965) inv	GRCh37 (hg19)		NC_000013.10	Chr13	48,773,377 (-211, +211)	48,780,754 (-211, +211)
essv14716030	Submitted genomic		NC_000013.10:g.(48 773166_48773588)_( 48780543_48780965) inv	GRCh37 (hg19)		NC_000013.10	Chr13	48,773,377 (-211, +211)	48,780,754 (-211, +211)
essv14716031	Submitted genomic		NC_000013.10:g.(48 773166_48773588)_( 48780543_48780965) inv	GRCh37 (hg19)		NC_000013.10	Chr13	48,773,377 (-211, +211)	48,780,754 (-211, +211)
essv14716032	Submitted genomic		NC_000013.10:g.(48 773166_48773588)_( 48780543_48780965) inv	GRCh37 (hg19)		NC_000013.10	Chr13	48,773,377 (-211, +211)	48,780,754 (-211, +211)
essv14716033	Submitted genomic		NC_000013.10:g.(48 773166_48773588)_( 48780543_48780965) inv	GRCh37 (hg19)		NC_000013.10	Chr13	48,773,377 (-211, +211)	48,780,754 (-211, +211)
essv14716034	Submitted genomic		NC_000013.10:g.(48 773166_48773588)_( 48780543_48780965) inv	GRCh37 (hg19)		NC_000013.10	Chr13	48,773,377 (-211, +211)	48,780,754 (-211, +211)
essv14716035	Submitted genomic		NC_000013.10:g.(48 773166_48773588)_( 48780543_48780965) inv	GRCh37 (hg19)		NC_000013.10	Chr13	48,773,377 (-211, +211)	48,780,754 (-211, +211)
essv14716036	Submitted genomic		NC_000013.10:g.(48 773166_48773588)_( 48780543_48780965) inv	GRCh37 (hg19)		NC_000013.10	Chr13	48,773,377 (-211, +211)	48,780,754 (-211, +211)
essv14716037	Submitted genomic		NC_000013.10:g.(48 773166_48773588)_( 48780543_48780965) inv	GRCh37 (hg19)		NC_000013.10	Chr13	48,773,377 (-211, +211)	48,780,754 (-211, +211)
essv14716038	Submitted genomic		NC_000013.10:g.(48 773166_48773588)_( 48780543_48780965) inv	GRCh37 (hg19)		NC_000013.10	Chr13	48,773,377 (-211, +211)	48,780,754 (-211, +211)
essv14716039	Submitted genomic		NC_000013.10:g.(48 773166_48773588)_( 48780543_48780965) inv	GRCh37 (hg19)		NC_000013.10	Chr13	48,773,377 (-211, +211)	48,780,754 (-211, +211)
essv14716040	Submitted genomic		NC_000013.10:g.(48 773166_48773588)_( 48780543_48780965) inv	GRCh37 (hg19)		NC_000013.10	Chr13	48,773,377 (-211, +211)	48,780,754 (-211, +211)
essv14716041	Submitted genomic		NC_000013.10:g.(48 773166_48773588)_( 48780543_48780965) inv	GRCh37 (hg19)		NC_000013.10	Chr13	48,773,377 (-211, +211)	48,780,754 (-211, +211)
essv14716042	Submitted genomic		NC_000013.10:g.(48 773166_48773588)_( 48780543_48780965) inv	GRCh37 (hg19)		NC_000013.10	Chr13	48,773,377 (-211, +211)	48,780,754 (-211, +211)
essv14716043	Submitted genomic		NC_000013.10:g.(48 773166_48773588)_( 48780543_48780965) inv	GRCh37 (hg19)		NC_000013.10	Chr13	48,773,377 (-211, +211)	48,780,754 (-211, +211)
essv14716044	Submitted genomic		NC_000013.10:g.(48 773166_48773588)_( 48780543_48780965) inv	GRCh37 (hg19)		NC_000013.10	Chr13	48,773,377 (-211, +211)	48,780,754 (-211, +211)
essv14716045	Submitted genomic		NC_000013.10:g.(48 773166_48773588)_( 48780543_48780965) inv	GRCh37 (hg19)		NC_000013.10	Chr13	48,773,377 (-211, +211)	48,780,754 (-211, +211)
essv14716046	Submitted genomic		NC_000013.10:g.(48 773166_48773588)_( 48780543_48780965) inv	GRCh37 (hg19)		NC_000013.10	Chr13	48,773,377 (-211, +211)	48,780,754 (-211, +211)
essv14716047	Submitted genomic		NC_000013.10:g.(48 773166_48773588)_( 48780543_48780965) inv	GRCh37 (hg19)		NC_000013.10	Chr13	48,773,377 (-211, +211)	48,780,754 (-211, +211)
essv14716048	Submitted genomic		NC_000013.10:g.(48 773166_48773588)_( 48780543_48780965) inv	GRCh37 (hg19)		NC_000013.10	Chr13	48,773,377 (-211, +211)	48,780,754 (-211, +211)
essv14716049	Submitted genomic		NC_000013.10:g.(48 773166_48773588)_( 48780543_48780965) inv	GRCh37 (hg19)		NC_000013.10	Chr13	48,773,377 (-211, +211)	48,780,754 (-211, +211)
essv14716050	Submitted genomic		NC_000013.10:g.(48 773166_48773588)_( 48780543_48780965) inv	GRCh37 (hg19)		NC_000013.10	Chr13	48,773,377 (-211, +211)	48,780,754 (-211, +211)
essv14716051	Submitted genomic		NC_000013.10:g.(48 773166_48773588)_( 48780543_48780965) inv	GRCh37 (hg19)		NC_000013.10	Chr13	48,773,377 (-211, +211)	48,780,754 (-211, +211)
essv14716052	Submitted genomic		NC_000013.10:g.(48 773166_48773588)_( 48780543_48780965) inv	GRCh37 (hg19)		NC_000013.10	Chr13	48,773,377 (-211, +211)	48,780,754 (-211, +211)
essv14716053	Submitted genomic		NC_000013.10:g.(48 773166_48773588)_( 48780543_48780965) inv	GRCh37 (hg19)		NC_000013.10	Chr13	48,773,377 (-211, +211)	48,780,754 (-211, +211)
essv14716054	Submitted genomic		NC_000013.10:g.(48 773166_48773588)_( 48780543_48780965) inv	GRCh37 (hg19)		NC_000013.10	Chr13	48,773,377 (-211, +211)	48,780,754 (-211, +211)

dbVar

Database of genomic structural variation

esv3632019

Links to Other Resources

Genome View

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.