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dbVar

Database of genomic structural variation

nsv5908623

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:6,777

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: 120 SVs from 32 studies. See in: genome view

Submitted genomic83,052,801-83,059,577

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5908623	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	83,052,801	83,059,577
nsv5908623	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	82,682,117	82,688,893

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17431567	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17431567	Submitted genomic		NC_000007.14:g.830 52801_83059577del	GRCh38 (hg38)		NC_000007.14	Chr7	83,052,801	83,059,577
nssv17431567	Remapped	Perfect	NC_000007.13:g.826 82117_82688893del	GRCh37.p13	First Pass	NC_000007.13	Chr7	82,682,117	82,688,893

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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