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dbVar

Database of genomic structural variation

nsv5925458

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:8,978

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

Submitted genomic132,115,919-132,124,896

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5925458	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	132,115,919	132,124,896
nsv5925458	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	131,800,678	131,809,655

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17437754	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17437754	Submitted genomic		NC_000007.14:g.132 115919_132124896de l	GRCh38 (hg38)		NC_000007.14	Chr7	132,115,919	132,124,896
nssv17437754	Remapped	Perfect	NC_000007.13:g.131 800678_131809655de l	GRCh37.p13	First Pass	NC_000007.13	Chr7	131,800,678	131,809,655

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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