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dbVar

Database of genomic structural variation

nsv5979992

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: 307 SVs from 33 studies. See in: genome view

Submitted genomic132,071,853-132,071,853

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5979992	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000010.11	Chr10	132,071,853	132,071,853
nsv5979992	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000010.10	Chr10	133,885,357	133,885,357

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17359880	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17359880	Submitted genomic		NC_000010.11:g.132 071853_132071854in s57	GRCh38 (hg38)		NC_000010.11	Chr10	132,071,853	132,071,853
nssv17359880	Remapped	Perfect	NC_000010.10:g.133 885357_133885358in s57	GRCh37.p13	First Pass	NC_000010.10	Chr10	133,885,357	133,885,357

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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