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dbVar

Database of genomic structural variation

nsv5951025

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: 151 SVs from 40 studies. See in: genome view

Submitted genomic71,204,026-71,204,026

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5951025	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	71,204,026	71,204,026
nsv5951025	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	70,669,012	70,669,012

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17435951	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17435951	Submitted genomic		NC_000007.14:g.712 04026_71204027ins3 26	GRCh38 (hg38)		NC_000007.14	Chr7	71,204,026	71,204,026
nssv17435951	Remapped	Perfect	NC_000007.13:g.706 69012_70669013ins3 26	GRCh37.p13	First Pass	NC_000007.13	Chr7	70,669,012	70,669,012

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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