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dbVar

Database of genomic structural variation

nsv5917279

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:159

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: 201 SVs from 22 studies. See in: genome view

Submitted genomic133,777,332-133,777,490

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5917279	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000008.11	Chr8	133,777,332	133,777,490
nsv5917279	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000008.10	Chr8	134,789,575	134,789,733

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17447736	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17447736	Submitted genomic		NC_000008.11:g.133 777332_133777490de l	GRCh38 (hg38)		NC_000008.11	Chr8	133,777,332	133,777,490
nssv17447736	Remapped	Perfect	NC_000008.10:g.134 789575_134789733de l	GRCh37.p13	First Pass	NC_000008.10	Chr8	134,789,575	134,789,733

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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