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dbVar

Database of genomic structural variation

nsv5915042

Organism: Homo sapiens

Study:nstd209 (Almarri et al. 2020)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:75

Publication(s):Almarri et al. 2020

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: 177 SVs from 38 studies. See in: genome view

Submitted genomic71,604,174-71,604,248

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5915042	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	71,604,174	71,604,248
nsv5915042	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	71,069,159	71,069,233

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17449375	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17449375	Submitted genomic		NC_000007.14:g.716 04174_71604248del	GRCh38 (hg38)		NC_000007.14	Chr7	71,604,174	71,604,248
nssv17449375	Remapped	Perfect	NC_000007.13:g.710 69159_71069233del	GRCh37.p13	First Pass	NC_000007.13	Chr7	71,069,159	71,069,233

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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