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dbVar

Database of genomic structural variation

nsv5894046

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:1,323

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

Submitted genomic231,105,479-231,106,801

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5894046	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	231,105,479	231,106,801
nsv5894046	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	231,970,193	231,971,515

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17406134	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17406134	Submitted genomic		NC_000002.12:g.231 105479_231106801de l	GRCh38 (hg38)		NC_000002.12	Chr2	231,105,479	231,106,801
nssv17406134	Remapped	Perfect	NC_000002.11:g.231 970193_231971515de l	GRCh37.p13	First Pass	NC_000002.11	Chr2	231,970,193	231,971,515

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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