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dbVar

Database of genomic structural variation

nsv5980347

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: 189 SVs from 28 studies. See in: genome view

Submitted genomic124,639,122-124,639,122

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5980347	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000010.11	Chr10	124,639,122	124,639,122
nsv5980347	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000010.10	Chr10	126,327,691	126,327,691

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17350428	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17350428	Submitted genomic		NC_000010.11:g.124 639122_124639123in s200	GRCh38 (hg38)		NC_000010.11	Chr10	124,639,122	124,639,122
nssv17350428	Remapped	Perfect	NC_000010.10:g.126 327691_126327692in s200	GRCh37.p13	First Pass	NC_000010.10	Chr10	126,327,691	126,327,691

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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