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dbVar

Database of genomic structural variation

nsv5603917

Organism: Homo sapiens

Study:nstd207 (Ebert et al. 2021)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:4,733

Publication(s):Ebert et al. 2021

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: 120 SVs from 28 studies. See in: genome view

Submitted genomic81,988,169-81,992,901

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5603917	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000009.12	Chr9	81,988,169	81,992,901
nsv5603917	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000009.11	Chr9	84,603,084	84,607,816

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17162689	deletion	HG03065	Sequencing	Sequence alignment	3,836

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17162689	Submitted genomic		NC_000009.12:g.819 88169_81992901delT	GRCh38 (hg38)		NC_000009.12	Chr9	81,988,169	81,992,901
nssv17162689	Remapped	Perfect	NC_000009.11:g.846 03084_84607816delT	GRCh37.p13	First Pass	NC_000009.11	Chr9	84,603,084	84,607,816

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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