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dbVar

Database of genomic structural variation

nsv5583137

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:58

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

Submitted genomic39,272,001-39,272,058

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5583137	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000005.10	Chr5	39,272,001	39,272,058
nsv5583137	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000005.9	Chr5	39,272,103	39,272,160

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17136141	deletion	HG00512	Sequencing	Sequence alignment	6,637

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17136141	Submitted genomic		NC_000005.10:g.392 72001_39272058delA	GRCh38 (hg38)		NC_000005.10	Chr5	39,272,001	39,272,058
nssv17136141	Remapped	Perfect	NC_000005.9:g.3927 2103_39272160delA	GRCh37.p13	First Pass	NC_000005.9	Chr5	39,272,103	39,272,160

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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