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

dbVar

Database of genomic structural variation

nsv5615086

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

Submitted genomic17,191,906-17,191,906

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5615086	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000001.11	Chr1	17,191,906	17,191,906
nsv5615086	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	17,518,401	17,518,401

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17061909	insertion	NA24385	Sequencing	Sequence alignment	2,573

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17061909	Submitted genomic		NC_000001.11:g.171 91906_17191907ins6 1	GRCh38 (hg38)		NC_000001.11	Chr1	17,191,906	17,191,906
nssv17061909	Remapped	Perfect	NC_000001.10:g.175 18401_17518402ins6 1	GRCh37.p13	First Pass	NC_000001.10	Chr1	17,518,401	17,518,401

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