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dbVar

Database of genomic structural variation

nsv5926052

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:56

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: 116 SVs from 25 studies. See in: genome view

Submitted genomic130,164,421-130,164,476

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5926052	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	130,164,421	130,164,476
nsv5926052	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	129,804,261	129,804,316

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17438094	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17438094	Submitted genomic		NC_000007.14:g.130 164421_130164476de l	GRCh38 (hg38)		NC_000007.14	Chr7	130,164,421	130,164,476
nssv17438094	Remapped	Perfect	NC_000007.13:g.129 804261_129804316de l	GRCh37.p13	First Pass	NC_000007.13	Chr7	129,804,261	129,804,316

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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