nsv3326421

Organism: Homo sapiens

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

Variant Calls:10
Validation:Not tested
Clinical Assertions: No
Region Size:8,118

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

Genome View

Select assembly:

Overlapping variant regions from other studies: 393 SVs from 62 studies. See in: genome view

Submitted genomic122,600,825-122,608,942

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv3326421	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000010.11	Chr10	122,600,825	122,608,942
nsv3326421	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000010.10	Chr10	124,360,341	124,368,458

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv14494782	deletion	SAMN02744161	Sequencing	de novo and local sequence assembly	20,941
nssv14496422	deletion	SAMN09651199	Sequencing	de novo and local sequence assembly	27,381
nssv14498981	deletion	SAMN09643900	Sequencing	de novo and local sequence assembly	26,631
nssv14500261	deletion	SAMN03255769	Sequencing	de novo and local sequence assembly	21,134
nssv14505105	deletion	SAMN06885952	Sequencing	de novo and local sequence assembly	28,070
nssv14505459	deletion	SAMN04229548	Sequencing	de novo and local sequence assembly	23,009
nssv14505635	deletion	SAMN04251426	Sequencing	de novo and local sequence assembly	22,074
nssv14505892	deletion	SAMN04229552	Sequencing	de novo and local sequence assembly	24,632
nssv14510163	deletion	SAMN09690649	Sequencing	de novo and local sequence assembly	21,495
nssv14511074	deletion	SAMN05603745	Sequencing	de novo and local sequence assembly	27,447

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv14494782	Submitted genomic		NC_000010.11:g.122 600825_122608942de l	GRCh38 (hg38)		NC_000010.11	Chr10	122,600,825	122,608,942
nssv14496422	Submitted genomic		NC_000010.11:g.122 600825_122608942de l	GRCh38 (hg38)		NC_000010.11	Chr10	122,600,825	122,608,942
nssv14498981	Submitted genomic		NC_000010.11:g.122 600825_122608942de l	GRCh38 (hg38)		NC_000010.11	Chr10	122,600,825	122,608,942
nssv14500261	Submitted genomic		NC_000010.11:g.122 600825_122608942de l	GRCh38 (hg38)		NC_000010.11	Chr10	122,600,825	122,608,942
nssv14505105	Submitted genomic		NC_000010.11:g.122 600825_122608942de l	GRCh38 (hg38)		NC_000010.11	Chr10	122,600,825	122,608,942
nssv14505459	Submitted genomic		NC_000010.11:g.122 600825_122608942de l	GRCh38 (hg38)		NC_000010.11	Chr10	122,600,825	122,608,942
nssv14505635	Submitted genomic		NC_000010.11:g.122 600825_122608942de l	GRCh38 (hg38)		NC_000010.11	Chr10	122,600,825	122,608,942
nssv14505892	Submitted genomic		NC_000010.11:g.122 600825_122608942de l	GRCh38 (hg38)		NC_000010.11	Chr10	122,600,825	122,608,942
nssv14510163	Submitted genomic		NC_000010.11:g.122 600825_122608942de l	GRCh38 (hg38)		NC_000010.11	Chr10	122,600,825	122,608,942
nssv14511074	Submitted genomic		NC_000010.11:g.122 600825_122608942de l	GRCh38 (hg38)		NC_000010.11	Chr10	122,600,825	122,608,942
nssv14494782	Remapped	Perfect	NC_000010.10:g.124 360341_124368458de lNC_000010.10:g.12 4360341_124368458d el	GRCh37.p13	First Pass	NC_000010.10	Chr10	124,360,341	124,368,458
nssv14496422	Remapped	Perfect	NC_000010.10:g.124 360341_124368458de lNC_000010.10:g.12 4360341_124368458d el	GRCh37.p13	First Pass	NC_000010.10	Chr10	124,360,341	124,368,458
nssv14498981	Remapped	Perfect	NC_000010.10:g.124 360341_124368458de lNC_000010.10:g.12 4360341_124368458d el	GRCh37.p13	First Pass	NC_000010.10	Chr10	124,360,341	124,368,458
nssv14500261	Remapped	Perfect	NC_000010.10:g.124 360341_124368458de lNC_000010.10:g.12 4360341_124368458d el	GRCh37.p13	First Pass	NC_000010.10	Chr10	124,360,341	124,368,458
nssv14505105	Remapped	Perfect	NC_000010.10:g.124 360341_124368458de lNC_000010.10:g.12 4360341_124368458d el	GRCh37.p13	First Pass	NC_000010.10	Chr10	124,360,341	124,368,458
nssv14505459	Remapped	Perfect	NC_000010.10:g.124 360341_124368458de lNC_000010.10:g.12 4360341_124368458d el	GRCh37.p13	First Pass	NC_000010.10	Chr10	124,360,341	124,368,458
nssv14505635	Remapped	Perfect	NC_000010.10:g.124 360341_124368458de lNC_000010.10:g.12 4360341_124368458d el	GRCh37.p13	First Pass	NC_000010.10	Chr10	124,360,341	124,368,458
nssv14505892	Remapped	Perfect	NC_000010.10:g.124 360341_124368458de lNC_000010.10:g.12 4360341_124368458d el	GRCh37.p13	First Pass	NC_000010.10	Chr10	124,360,341	124,368,458
nssv14510163	Remapped	Perfect	NC_000010.10:g.124 360341_124368458de lNC_000010.10:g.12 4360341_124368458d el	GRCh37.p13	First Pass	NC_000010.10	Chr10	124,360,341	124,368,458
nssv14511074	Remapped	Perfect	NC_000010.10:g.124 360341_124368458de lNC_000010.10:g.12 4360341_124368458d el	GRCh37.p13	First Pass	NC_000010.10	Chr10	124,360,341	124,368,458

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dbVar

Database of genomic structural variation

nsv3326421

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

No genotype data were submitted for this variant