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dbVar

Database of genomic structural variation

nsv5924585

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:183

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

Submitted genomic135,096,480-135,096,662

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5924585	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	135,096,480	135,096,662
nsv5924585	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	134,781,232	134,781,414

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17446645	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17446645	Submitted genomic		NC_000007.14:g.135 096480_135096662de l	GRCh38 (hg38)		NC_000007.14	Chr7	135,096,480	135,096,662
nssv17446645	Remapped	Perfect	NC_000007.13:g.134 781232_134781414de l	GRCh37.p13	First Pass	NC_000007.13	Chr7	134,781,232	134,781,414

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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