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dbVar

Database of genomic structural variation

nsv5906645

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:60

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: 166 SVs from 42 studies. See in: genome view

Submitted genomic73,158,131-73,158,190

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5906645	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000004.12	Chr4	73,158,131	73,158,190
nsv5906645	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000004.11	Chr4	74,023,848	74,023,907

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17422144	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17422144	Submitted genomic		NC_000004.12:g.731 58131_73158190del	GRCh38 (hg38)		NC_000004.12	Chr4	73,158,131	73,158,190
nssv17422144	Remapped	Perfect	NC_000004.11:g.740 23848_74023907del	GRCh37.p13	First Pass	NC_000004.11	Chr4	74,023,848	74,023,907

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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