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dbVar

Database of genomic structural variation

nsv5890441

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:126

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: 138 SVs from 30 studies. See in: genome view

Submitted genomic121,384,019-121,384,144

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5890441	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	121,384,019	121,384,144
nsv5890441	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	122,141,595	122,141,720

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17403380	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17403380	Submitted genomic		NC_000002.12:g.121 384019_121384144de l	GRCh38 (hg38)		NC_000002.12	Chr2	121,384,019	121,384,144
nssv17403380	Remapped	Perfect	NC_000002.11:g.122 141595_122141720de l	GRCh37.p13	First Pass	NC_000002.11	Chr2	122,141,595	122,141,720

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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