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dbVar

Database of genomic structural variation

nsv5955798

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: 98 SVs from 17 studies. See in: genome view

Submitted genomic130,953,995-130,953,995

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5955798	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	130,953,995	130,953,995
nsv5955798	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	131,275,135	131,275,135

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17425919	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17425919	Submitted genomic		NC_000006.12:g.130 953995_130953996in s237	GRCh38 (hg38)		NC_000006.12	Chr6	130,953,995	130,953,995
nssv17425919	Remapped	Perfect	NC_000006.11:g.131 275135_131275136in s237	GRCh37.p13	First Pass	NC_000006.11	Chr6	131,275,135	131,275,135

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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