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dbVar

Database of genomic structural variation

nsv5885356

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:265

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 22 studies. See in: genome view

Submitted genomic11,973,736-11,974,000

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5885356	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000001.11	Chr1	11,973,736	11,974,000
nsv5885356	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	12,033,793	12,034,057

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17359543	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17359543	Submitted genomic		NC_000001.11:g.119 73736_11974000del	GRCh38 (hg38)		NC_000001.11	Chr1	11,973,736	11,974,000
nssv17359543	Remapped	Perfect	NC_000001.10:g.120 33793_12034057del	GRCh37.p13	First Pass	NC_000001.10	Chr1	12,033,793	12,034,057

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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