nsv3332255

Organism: Homo sapiens

Study:nstd162 (Audano et al. 2019)
Variant Type:inversion
Method Type:Sequencing
Submitted on:GRCh38 (hg38)

Variant Calls:14
Validation:Not tested
Clinical Assertions: No
Region Size:19,410

Publication(s):Audano et al. 2019

Links to Other Resources

Overlapping Genes

Source: NCBI

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

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Select assembly:

Overlapping variant regions from other studies: 596 SVs from 81 studies. See in: genome view

Submitted genomic49,711,900-49,731,309

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv3332255	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000011.10	Chr11	49,711,900	49,731,309
nsv3332255	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	49,733,452	49,752,861

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv14512846	inversion	SAMN09690649	Sequencing	de novo and local sequence assembly	21,495
nssv14513076	inversion	SAMN05603847	Sequencing	de novo and local sequence assembly	26,021
nssv14513493	inversion	SAMN05181962	Sequencing	de novo and local sequence assembly	23,563
nssv14514246	inversion	SAMN04229552	Sequencing	de novo and local sequence assembly	24,632
nssv14515601	inversion	SAMN04251426	Sequencing	de novo and local sequence assembly	22,074
nssv14520259	inversion	SAMN03838746	Sequencing	de novo and local sequence assembly	26,336
nssv14520848	inversion	SAMN05603729	Sequencing	de novo and local sequence assembly	24,108
nssv14521223	inversion	SAMN06885952	Sequencing	de novo and local sequence assembly	28,070
nssv14521395	inversion	SAMN04229548	Sequencing	de novo and local sequence assembly	23,009
nssv14521869	inversion	SAMN09643900	Sequencing	de novo and local sequence assembly	26,631
nssv14523444	inversion	SAMN09651199	Sequencing	de novo and local sequence assembly	27,381
nssv14525637	inversion	SAMN05603745	Sequencing	de novo and local sequence assembly	27,447
nssv14526137	inversion	SAMN03255769	Sequencing	de novo and local sequence assembly	21,134
nssv14529555	inversion	SAMN02744161	Sequencing	de novo and local sequence assembly	20,941

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv14512846	Submitted genomic		NC_000011.10:g.497 11900_49731309inv	GRCh38 (hg38)		NC_000011.10	Chr11	49,711,900	49,731,309
nssv14513076	Submitted genomic		NC_000011.10:g.497 11900_49731309inv	GRCh38 (hg38)		NC_000011.10	Chr11	49,711,900	49,731,309
nssv14513493	Submitted genomic		NC_000011.10:g.497 11900_49731309inv	GRCh38 (hg38)		NC_000011.10	Chr11	49,711,900	49,731,309
nssv14514246	Submitted genomic		NC_000011.10:g.497 11900_49731309inv	GRCh38 (hg38)		NC_000011.10	Chr11	49,711,900	49,731,309
nssv14515601	Submitted genomic		NC_000011.10:g.497 11900_49731309inv	GRCh38 (hg38)		NC_000011.10	Chr11	49,711,900	49,731,309
nssv14520259	Submitted genomic		NC_000011.10:g.497 11900_49731309inv	GRCh38 (hg38)		NC_000011.10	Chr11	49,711,900	49,731,309
nssv14520848	Submitted genomic		NC_000011.10:g.497 11900_49731309inv	GRCh38 (hg38)		NC_000011.10	Chr11	49,711,900	49,731,309
nssv14521223	Submitted genomic		NC_000011.10:g.497 11900_49731309inv	GRCh38 (hg38)		NC_000011.10	Chr11	49,711,900	49,731,309
nssv14521395	Submitted genomic		NC_000011.10:g.497 11900_49731309inv	GRCh38 (hg38)		NC_000011.10	Chr11	49,711,900	49,731,309
nssv14521869	Submitted genomic		NC_000011.10:g.497 11900_49731309inv	GRCh38 (hg38)		NC_000011.10	Chr11	49,711,900	49,731,309
nssv14523444	Submitted genomic		NC_000011.10:g.497 11900_49731309inv	GRCh38 (hg38)		NC_000011.10	Chr11	49,711,900	49,731,309
nssv14525637	Submitted genomic		NC_000011.10:g.497 11900_49731309inv	GRCh38 (hg38)		NC_000011.10	Chr11	49,711,900	49,731,309
nssv14526137	Submitted genomic		NC_000011.10:g.497 11900_49731309inv	GRCh38 (hg38)		NC_000011.10	Chr11	49,711,900	49,731,309
nssv14529555	Submitted genomic		NC_000011.10:g.497 11900_49731309inv	GRCh38 (hg38)		NC_000011.10	Chr11	49,711,900	49,731,309
nssv14512846	Remapped	Perfect	NC_000011.9:g.4973 3452_49752861invNC _000011.9:g.497334 52_49752861inv	GRCh37.p13	First Pass	NC_000011.9	Chr11	49,733,452	49,752,861
nssv14513076	Remapped	Perfect	NC_000011.9:g.4973 3452_49752861invNC _000011.9:g.497334 52_49752861inv	GRCh37.p13	First Pass	NC_000011.9	Chr11	49,733,452	49,752,861
nssv14513493	Remapped	Perfect	NC_000011.9:g.4973 3452_49752861invNC _000011.9:g.497334 52_49752861inv	GRCh37.p13	First Pass	NC_000011.9	Chr11	49,733,452	49,752,861
nssv14514246	Remapped	Perfect	NC_000011.9:g.4973 3452_49752861invNC _000011.9:g.497334 52_49752861inv	GRCh37.p13	First Pass	NC_000011.9	Chr11	49,733,452	49,752,861
nssv14515601	Remapped	Perfect	NC_000011.9:g.4973 3452_49752861invNC _000011.9:g.497334 52_49752861inv	GRCh37.p13	First Pass	NC_000011.9	Chr11	49,733,452	49,752,861
nssv14520259	Remapped	Perfect	NC_000011.9:g.4973 3452_49752861invNC _000011.9:g.497334 52_49752861inv	GRCh37.p13	First Pass	NC_000011.9	Chr11	49,733,452	49,752,861
nssv14520848	Remapped	Perfect	NC_000011.9:g.4973 3452_49752861invNC _000011.9:g.497334 52_49752861inv	GRCh37.p13	First Pass	NC_000011.9	Chr11	49,733,452	49,752,861
nssv14521223	Remapped	Perfect	NC_000011.9:g.4973 3452_49752861invNC _000011.9:g.497334 52_49752861inv	GRCh37.p13	First Pass	NC_000011.9	Chr11	49,733,452	49,752,861
nssv14521395	Remapped	Perfect	NC_000011.9:g.4973 3452_49752861invNC _000011.9:g.497334 52_49752861inv	GRCh37.p13	First Pass	NC_000011.9	Chr11	49,733,452	49,752,861
nssv14521869	Remapped	Perfect	NC_000011.9:g.4973 3452_49752861invNC _000011.9:g.497334 52_49752861inv	GRCh37.p13	First Pass	NC_000011.9	Chr11	49,733,452	49,752,861
nssv14523444	Remapped	Perfect	NC_000011.9:g.4973 3452_49752861invNC _000011.9:g.497334 52_49752861inv	GRCh37.p13	First Pass	NC_000011.9	Chr11	49,733,452	49,752,861
nssv14525637	Remapped	Perfect	NC_000011.9:g.4973 3452_49752861invNC _000011.9:g.497334 52_49752861inv	GRCh37.p13	First Pass	NC_000011.9	Chr11	49,733,452	49,752,861
nssv14526137	Remapped	Perfect	NC_000011.9:g.4973 3452_49752861invNC _000011.9:g.497334 52_49752861inv	GRCh37.p13	First Pass	NC_000011.9	Chr11	49,733,452	49,752,861
nssv14529555	Remapped	Perfect	NC_000011.9:g.4973 3452_49752861invNC _000011.9:g.497334 52_49752861inv	GRCh37.p13	First Pass	NC_000011.9	Chr11	49,733,452	49,752,861

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dbVar

Database of genomic structural variation

nsv3332255

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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

No genotype data were submitted for this variant