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dbVar

Database of genomic structural variation

nsv5921012

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:338

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: 168 SVs from 53 studies. See in: genome view

Submitted genomic106,093,544-106,093,881

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5921012	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	106,093,544	106,093,881
nsv5921012	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	105,733,990	105,734,327

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17443636	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17443636	Submitted genomic		NC_000007.14:g.106 093544_106093881de l	GRCh38 (hg38)		NC_000007.14	Chr7	106,093,544	106,093,881
nssv17443636	Remapped	Perfect	NC_000007.13:g.105 733990_105734327de l	GRCh37.p13	First Pass	NC_000007.13	Chr7	105,733,990	105,734,327

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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