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dbVar

Database of genomic structural variation

nsv5599767

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:52

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: 108 SVs from 27 studies. See in: genome view

Submitted genomic57,628,889-57,628,940

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5599767	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000016.10	Chr16	57,628,889	57,628,940
nsv5599767	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000016.9	Chr16	57,662,801	57,662,852

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17083485	deletion	HG02011	Sequencing	Sequence alignment	2,906

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17083485	Submitted genomic		NC_000016.10:g.576 28889_57628940delT	GRCh38 (hg38)		NC_000016.10	Chr16	57,628,889	57,628,940
nssv17083485	Remapped	Perfect	NC_000016.9:g.5766 2801_57662852delT	GRCh37.p13	First Pass	NC_000016.9	Chr16	57,662,801	57,662,852

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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