nsv3371532

Organism: Homo sapiens

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

Variant Calls:12
Validation:Not tested
Clinical Assertions: No
Region Size:13,625

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: 202 SVs from 43 studies. See in: genome view

Submitted genomic38,769,343-38,782,967

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv3371532	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	38,769,343	38,782,967
nsv3371532	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	39,259,983	39,273,607

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv14612518	inversion	SAMN04229552	Sequencing	de novo and local sequence assembly	24,632
nssv14616067	inversion	SAMN05603729	Sequencing	de novo and local sequence assembly	24,108
nssv14616376	inversion	SAMN09643900	Sequencing	de novo and local sequence assembly	26,631
nssv14618580	inversion	SAMN05181962	Sequencing	de novo and local sequence assembly	23,563
nssv14621751	inversion	SAMN06885952	Sequencing	de novo and local sequence assembly	28,070
nssv14621811	inversion	SAMN02744161	Sequencing	de novo and local sequence assembly	20,941
nssv14622559	inversion	SAMN03255769	Sequencing	de novo and local sequence assembly	21,134
nssv14628366	inversion	SAMN03838746	Sequencing	de novo and local sequence assembly	26,336
nssv14629304	inversion	SAMN09651199	Sequencing	de novo and local sequence assembly	27,381
nssv14629365	inversion	SAMN05603745	Sequencing	de novo and local sequence assembly	27,447
nssv14629700	inversion	SAMN05603847	Sequencing	de novo and local sequence assembly	26,021
nssv14629756	inversion	SAMN04251426	Sequencing	de novo and local sequence assembly	22,074

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv14612518	Submitted genomic		NC_000019.10:g.387 69343_38782967inv	GRCh38 (hg38)		NC_000019.10	Chr19	38,769,343	38,782,967
nssv14616067	Submitted genomic		NC_000019.10:g.387 69343_38782967inv	GRCh38 (hg38)		NC_000019.10	Chr19	38,769,343	38,782,967
nssv14616376	Submitted genomic		NC_000019.10:g.387 69343_38782967inv	GRCh38 (hg38)		NC_000019.10	Chr19	38,769,343	38,782,967
nssv14618580	Submitted genomic		NC_000019.10:g.387 69343_38782967inv	GRCh38 (hg38)		NC_000019.10	Chr19	38,769,343	38,782,967
nssv14621751	Submitted genomic		NC_000019.10:g.387 69343_38782967inv	GRCh38 (hg38)		NC_000019.10	Chr19	38,769,343	38,782,967
nssv14621811	Submitted genomic		NC_000019.10:g.387 69343_38782967inv	GRCh38 (hg38)		NC_000019.10	Chr19	38,769,343	38,782,967
nssv14622559	Submitted genomic		NC_000019.10:g.387 69343_38782967inv	GRCh38 (hg38)		NC_000019.10	Chr19	38,769,343	38,782,967
nssv14628366	Submitted genomic		NC_000019.10:g.387 69343_38782967inv	GRCh38 (hg38)		NC_000019.10	Chr19	38,769,343	38,782,967
nssv14629304	Submitted genomic		NC_000019.10:g.387 69343_38782967inv	GRCh38 (hg38)		NC_000019.10	Chr19	38,769,343	38,782,967
nssv14629365	Submitted genomic		NC_000019.10:g.387 69343_38782967inv	GRCh38 (hg38)		NC_000019.10	Chr19	38,769,343	38,782,967
nssv14629700	Submitted genomic		NC_000019.10:g.387 69343_38782967inv	GRCh38 (hg38)		NC_000019.10	Chr19	38,769,343	38,782,967
nssv14629756	Submitted genomic		NC_000019.10:g.387 69343_38782967inv	GRCh38 (hg38)		NC_000019.10	Chr19	38,769,343	38,782,967
nssv14612518	Remapped	Perfect	NC_000019.9:g.3925 9983_39273607invNC _000019.9:g.392599 83_39273607inv	GRCh37.p13	First Pass	NC_000019.9	Chr19	39,259,983	39,273,607
nssv14616067	Remapped	Perfect	NC_000019.9:g.3925 9983_39273607invNC _000019.9:g.392599 83_39273607inv	GRCh37.p13	First Pass	NC_000019.9	Chr19	39,259,983	39,273,607
nssv14616376	Remapped	Perfect	NC_000019.9:g.3925 9983_39273607invNC _000019.9:g.392599 83_39273607inv	GRCh37.p13	First Pass	NC_000019.9	Chr19	39,259,983	39,273,607
nssv14618580	Remapped	Perfect	NC_000019.9:g.3925 9983_39273607invNC _000019.9:g.392599 83_39273607inv	GRCh37.p13	First Pass	NC_000019.9	Chr19	39,259,983	39,273,607
nssv14621751	Remapped	Perfect	NC_000019.9:g.3925 9983_39273607invNC _000019.9:g.392599 83_39273607inv	GRCh37.p13	First Pass	NC_000019.9	Chr19	39,259,983	39,273,607
nssv14621811	Remapped	Perfect	NC_000019.9:g.3925 9983_39273607invNC _000019.9:g.392599 83_39273607inv	GRCh37.p13	First Pass	NC_000019.9	Chr19	39,259,983	39,273,607
nssv14622559	Remapped	Perfect	NC_000019.9:g.3925 9983_39273607invNC _000019.9:g.392599 83_39273607inv	GRCh37.p13	First Pass	NC_000019.9	Chr19	39,259,983	39,273,607
nssv14628366	Remapped	Perfect	NC_000019.9:g.3925 9983_39273607invNC _000019.9:g.392599 83_39273607inv	GRCh37.p13	First Pass	NC_000019.9	Chr19	39,259,983	39,273,607
nssv14629304	Remapped	Perfect	NC_000019.9:g.3925 9983_39273607invNC _000019.9:g.392599 83_39273607inv	GRCh37.p13	First Pass	NC_000019.9	Chr19	39,259,983	39,273,607
nssv14629365	Remapped	Perfect	NC_000019.9:g.3925 9983_39273607invNC _000019.9:g.392599 83_39273607inv	GRCh37.p13	First Pass	NC_000019.9	Chr19	39,259,983	39,273,607
nssv14629700	Remapped	Perfect	NC_000019.9:g.3925 9983_39273607invNC _000019.9:g.392599 83_39273607inv	GRCh37.p13	First Pass	NC_000019.9	Chr19	39,259,983	39,273,607
nssv14629756	Remapped	Perfect	NC_000019.9:g.3925 9983_39273607invNC _000019.9:g.392599 83_39273607inv	GRCh37.p13	First Pass	NC_000019.9	Chr19	39,259,983	39,273,607

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dbVar

Database of genomic structural variation

nsv3371532

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