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dbVar

Database of genomic structural variation

nsv5973387

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

Submitted genomic50,196,078-50,196,078

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5973387	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000015.10	Chr15	50,196,078	50,196,078
nsv5973387	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000015.9	Chr15	50,488,275	50,488,275

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17377521	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17377521	Submitted genomic		NC_000015.10:g.501 96078_50196079ins1 63	GRCh38 (hg38)		NC_000015.10	Chr15	50,196,078	50,196,078
nssv17377521	Remapped	Perfect	NC_000015.9:g.5048 8275_50488276ins16 3	GRCh37.p13	First Pass	NC_000015.9	Chr15	50,488,275	50,488,275

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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