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dbVar

Database of genomic structural variation

nsv5897050

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:3,215

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: 96 SVs from 22 studies. See in: genome view

Submitted genomic98,828,445-98,831,659

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5897050	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000003.12	Chr3	98,828,445	98,831,659
nsv5897050	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000003.11	Chr3	98,547,289	98,550,503

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17419000	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17419000	Submitted genomic		NC_000003.12:g.988 28445_98831659del	GRCh38 (hg38)		NC_000003.12	Chr3	98,828,445	98,831,659
nssv17419000	Remapped	Perfect	NC_000003.11:g.985 47289_98550503del	GRCh37.p13	First Pass	NC_000003.11	Chr3	98,547,289	98,550,503

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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