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dbVar

Database of genomic structural variation

nsv5946601

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:577,861

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: 2351 SVs from 91 studies. See in: genome view

Submitted genomic6,088,632-6,666,492

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5946601	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000016.10	Chr16	6,088,632	6,666,492
nsv5946601	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000016.9	Chr16	6,138,633	6,716,493

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17380656	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17380656	Submitted genomic		NC_000016.10:g.608 8632_6666492del	GRCh38 (hg38)		NC_000016.10	Chr16	6,088,632	6,666,492
nssv17380656	Remapped	Perfect	NC_000016.9:g.6138 633_6716493del	GRCh37.p13	First Pass	NC_000016.9	Chr16	6,138,633	6,716,493

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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