Warning: The NCBI web site requires JavaScript to function. more...

dbVar

Database of genomic structural variation

nsv5960751

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: 122 SVs from 30 studies. See in: genome view

Submitted genomic128,923,472-128,923,472

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5960751	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	128,923,472	128,923,472
nsv5960751	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	129,244,617	129,244,617

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17410132	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17410132	Submitted genomic		NC_000006.12:g.128 923472_128923473in s417	GRCh38 (hg38)		NC_000006.12	Chr6	128,923,472	128,923,472
nssv17410132	Remapped	Perfect	NC_000006.11:g.129 244617_129244618in s417	GRCh37.p13	First Pass	NC_000006.11	Chr6	129,244,617	129,244,617

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.

You are here: NCBI