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dbVar

Database of genomic structural variation

nsv5922049

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:78

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: 381 SVs from 35 studies. See in: genome view

Submitted genomic158,789,810-158,789,887

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5922049	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	158,789,810	158,789,887
nsv5922049	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	158,582,501	158,582,578

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17449334	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17449334	Submitted genomic		NC_000007.14:g.158 789810_158789887de l	GRCh38 (hg38)		NC_000007.14	Chr7	158,789,810	158,789,887
nssv17449334	Remapped	Perfect	NC_000007.13:g.158 582501_158582578de l	GRCh37.p13	First Pass	NC_000007.13	Chr7	158,582,501	158,582,578

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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