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dbVar

Database of genomic structural variation

nsv5976925

Organism: Homo sapiens

Study:nstd209 (Almarri et al. 2020)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:1

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: 127 SVs from 21 studies. See in: genome view

Submitted genomic49,652,608-49,652,608

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5976925	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000015.10	Chr15	49,652,608	49,652,608
nsv5976925	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000015.9	Chr15	49,944,805	49,944,805

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17381573	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17381573	Submitted genomic		NC_000015.10:g.496 52608_49652609ins6 5	GRCh38 (hg38)		NC_000015.10	Chr15	49,652,608	49,652,608
nssv17381573	Remapped	Perfect	NC_000015.9:g.4994 4805_49944806ins65	GRCh37.p13	First Pass	NC_000015.9	Chr15	49,944,805	49,944,805

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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