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dbVar

Database of genomic structural variation

nsv5893133

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:53

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: 333 SVs from 56 studies. See in: genome view

Submitted genomic675,815-675,867

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5893133	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	675,815	675,867
nsv5893133	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	675,815	675,867

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17434870	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17434870	Submitted genomic		NC_000006.12:g.675 815_675867del	GRCh38 (hg38)		NC_000006.12	Chr6	675,815	675,867
nssv17434870	Remapped	Perfect	NC_000006.11:g.675 815_675867del	GRCh37.p13	First Pass	NC_000006.11	Chr6	675,815	675,867

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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