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

dbVar

Database of genomic structural variation

nsv5656848

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: 368 SVs from 39 studies. See in: genome view

Submitted genomic17,077,752-17,077,752

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5656848	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000017.11	Chr17	17,077,752	17,077,752
nsv5656848	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000017.10	Chr17	16,981,066	16,981,066

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17090034	insertion	HG02011	Sequencing	Sequence alignment	2,906

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17090034	Submitted genomic		NC_000017.11:g.170 77752_17077753ins3 17	GRCh38 (hg38)		NC_000017.11	Chr17	17,077,752	17,077,752
nssv17090034	Remapped	Perfect	NC_000017.10:g.169 81066_16981067ins3 17	GRCh37.p13	First Pass	NC_000017.10	Chr17	16,981,066	16,981,066

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