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dbVar

Database of genomic structural variation

nsv5922688

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:161

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: 213 SVs from 24 studies. See in: genome view

Submitted genomic166,925,011-166,925,171

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5922688	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	166,925,011	166,925,171
nsv5922688	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	167,338,499	167,338,659

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17424955	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17424955	Submitted genomic		NC_000006.12:g.166 925011_166925171de l	GRCh38 (hg38)		NC_000006.12	Chr6	166,925,011	166,925,171
nssv17424955	Remapped	Perfect	NC_000006.11:g.167 338499_167338659de l	GRCh37.p13	First Pass	NC_000006.11	Chr6	167,338,499	167,338,659

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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