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dbVar

Database of genomic structural variation

nsv5961951

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: 141 SVs from 26 studies. See in: genome view

Submitted genomic132,519,499-132,519,499

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5961951	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000009.12	Chr9	132,519,499	132,519,499
nsv5961951	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000009.11	Chr9	135,394,886	135,394,886

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17447352	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17447352	Submitted genomic		NC_000009.12:g.132 519499_132519500in s200	GRCh38 (hg38)		NC_000009.12	Chr9	132,519,499	132,519,499
nssv17447352	Remapped	Perfect	NC_000009.11:g.135 394886_135394887in s200	GRCh37.p13	First Pass	NC_000009.11	Chr9	135,394,886	135,394,886

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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