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dbVar

Database of genomic structural variation

nsv5891559

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:1,288

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

Submitted genomic149,835,627-149,836,914

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5891559	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	149,835,627	149,836,914
nsv5891559	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	150,156,763	150,158,050

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17423096	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17423096	Submitted genomic		NC_000006.12:g.149 835627_149836914de l	GRCh38 (hg38)		NC_000006.12	Chr6	149,835,627	149,836,914
nssv17423096	Remapped	Perfect	NC_000006.11:g.150 156763_150158050de l	GRCh37.p13	First Pass	NC_000006.11	Chr6	150,156,763	150,158,050

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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