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

dbVar

Database of genomic structural variation

nsv5607661

Organism: Homo sapiens

Study:nstd207 (Ebert et al. 2021)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:1

Publication(s):Ebert et al. 2021

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: 149 SVs from 27 studies. See in: genome view

Submitted genomic201,339,055-201,339,055

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5607661	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	201,339,055	201,339,055
nsv5607661	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	202,203,778	202,203,778

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17111387	insertion	HG03371	Sequencing	Sequence alignment	2,852

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17111387	Submitted genomic		NC_000002.12:g.201 339055_201339056in s129	GRCh38 (hg38)		NC_000002.12	Chr2	201,339,055	201,339,055
nssv17111387	Remapped	Perfect	NC_000002.11:g.202 203778_202203779in s129	GRCh37.p13	First Pass	NC_000002.11	Chr2	202,203,778	202,203,778

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