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dbVar

Database of genomic structural variation

nsv5911338

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:500,092

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: 1753 SVs from 89 studies. See in: genome view

Submitted genomic128,499,612-128,999,703

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5911338	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	128,499,612	128,999,703
nsv5911338	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	128,139,666	128,639,757

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17446281	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17446281	Submitted genomic		NC_000007.14:g.128 499612_128999703de l	GRCh38 (hg38)		NC_000007.14	Chr7	128,499,612	128,999,703
nssv17446281	Remapped	Perfect	NC_000007.13:g.128 139666_128639757de l	GRCh37.p13	First Pass	NC_000007.13	Chr7	128,139,666	128,639,757

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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