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dbVar

Database of genomic structural variation

nsv5921754

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:700

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

Submitted genomic71,435,752-71,436,451

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5921754	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	71,435,752	71,436,451
nsv5921754	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	70,900,737	70,901,436

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17446703	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17446703	Submitted genomic		NC_000007.14:g.714 35752_71436451del	GRCh38 (hg38)		NC_000007.14	Chr7	71,435,752	71,436,451
nssv17446703	Remapped	Perfect	NC_000007.13:g.709 00737_70901436del	GRCh37.p13	First Pass	NC_000007.13	Chr7	70,900,737	70,901,436

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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