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dbVar

Database of genomic structural variation

nsv5924446

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:1,001

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: 173 SVs from 36 studies. See in: genome view

Submitted genomic71,596,245-71,597,245

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5924446	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	71,596,245	71,597,245
nsv5924446	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	71,061,230	71,062,230

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17443625	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17443625	Submitted genomic		NC_000007.14:g.715 96245_71597245del	GRCh38 (hg38)		NC_000007.14	Chr7	71,596,245	71,597,245
nssv17443625	Remapped	Perfect	NC_000007.13:g.710 61230_71062230del	GRCh37.p13	First Pass	NC_000007.13	Chr7	71,061,230	71,062,230

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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