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

dbVar

Database of genomic structural variation

nsv5655607

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

Submitted genomic81,426,451-81,426,451

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5655607	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000017.11	Chr17	81,426,451	81,426,451
nsv5655607	Remapped	Perfect	GRCh37.p13	PATCHES	First Pass	NW_003871087.1	Chr17\|NW_0 03871087.1	81,089	81,089

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17081077	insertion	HG03065	Sequencing	Sequence alignment	3,836

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17081077	Submitted genomic		NC_000017.11:g.814 26451_81426452ins2 70	GRCh38 (hg38)		NC_000017.11	Chr17	81,426,451	81,426,451
nssv17081077	Remapped	Perfect	NW_003871087.1:g.8 1089_81090ins270	GRCh37.p13	First Pass	NW_003871087.1	Chr17\|NW_0 03871087.1	81,089	81,089

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