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dbVar

Database of genomic structural variation

nsv5972456

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: 316 SVs from 38 studies. See in: genome view

Submitted genomic131,176,845-131,176,845

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5972456	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000010.11	Chr10	131,176,845	131,176,845
nsv5972456	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000010.10	Chr10	132,975,108	132,975,108

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17361535	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17361535	Submitted genomic		NC_000010.11:g.131 176845_131176846in s144	GRCh38 (hg38)		NC_000010.11	Chr10	131,176,845	131,176,845
nssv17361535	Remapped	Perfect	NC_000010.10:g.132 975108_132975109in s144	GRCh37.p13	First Pass	NC_000010.10	Chr10	132,975,108	132,975,108

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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