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dbVar

Database of genomic structural variation

nsv5886967

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:108

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: 156 SVs from 37 studies. See in: genome view

Submitted genomic24,251,385-24,251,492

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5886967	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	24,251,385	24,251,492
nsv5886967	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	24,474,254	24,474,361

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17389997	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17389997	Submitted genomic		NC_000002.12:g.242 51385_24251492del	GRCh38 (hg38)		NC_000002.12	Chr2	24,251,385	24,251,492
nssv17389997	Remapped	Perfect	NC_000002.11:g.244 74254_24474361del	GRCh37.p13	First Pass	NC_000002.11	Chr2	24,474,254	24,474,361

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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