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dbVar

Database of genomic structural variation

nsv5932694

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:6,118

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: 336 SVs from 35 studies. See in: genome view

Submitted genomic12,667,505-12,673,622

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5932694	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000018.10	Chr18	12,667,505	12,673,622
nsv5932694	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000018.9	Chr18	12,667,504	12,673,621

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17387164	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17387164	Submitted genomic		NC_000018.10:g.126 67505_12673622del	GRCh38 (hg38)		NC_000018.10	Chr18	12,667,505	12,673,622
nssv17387164	Remapped	Perfect	NC_000018.9:g.1266 7504_12673621del	GRCh37.p13	First Pass	NC_000018.9	Chr18	12,667,504	12,673,621

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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