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dbVar

Database of genomic structural variation

nsv5577608

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:1,642

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: 185 SVs from 34 studies. See in: genome view

Submitted genomic37,958,335-37,959,976

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5577608	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	37,958,335	37,959,976
nsv5577608	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	38,185,478	38,187,119

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17113149	deletion	HG03486	Sequencing	Sequence alignment	4,355

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17113149	Submitted genomic		NC_000002.12:g.379 58335_37959976delT	GRCh38 (hg38)		NC_000002.12	Chr2	37,958,335	37,959,976
nssv17113149	Remapped	Perfect	NC_000002.11:g.381 85478_38187119delT	GRCh37.p13	First Pass	NC_000002.11	Chr2	38,185,478	38,187,119

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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