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dbVar

Database of genomic structural variation

nsv2799997

Organism: Homo sapiens

Study:nstd137 (Huddleston et al. 2016)
Variant Type:inversion
Method Type:Sequencing
Submitted on:GRCh38 (hg38)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:13,625

Publication(s):Huddleston et al. 2016

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: 204 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
nsv2799997	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	38,769,343	38,782,967
nsv2799997	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
nssv13709037	inversion	SAMN02744161	Sequencing	Local sequence assembly	47

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv13709037	Submitted genomic		NC_000019.10:g.387 69343_38782967inv	GRCh38 (hg38)		NC_000019.10	Chr19	38,769,343	38,782,967
nssv13709037	Remapped	Perfect	NC_000019.9:g.3925 9983_39273607inv	GRCh37.p13	First Pass	NC_000019.9	Chr19	39,259,983	39,273,607

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.

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