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

dbVar

Database of genomic structural variation

nsv5653420

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: 291 SVs from 57 studies. See in: genome view

Submitted genomic72,061,419-72,061,419

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5653420	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000016.10	Chr16	72,061,419	72,061,419
nsv5653420	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000016.9	Chr16	72,095,318	72,095,318

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17080874	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
nssv17080874	Submitted genomic		NC_000016.10:g.720 61419_72061420ins3 2374	GRCh38 (hg38)		NC_000016.10	Chr16	72,061,419	72,061,419
nssv17080874	Remapped	Perfect	NC_000016.9:g.7209 5318_72095319ins32 374	GRCh37.p13	First Pass	NC_000016.9	Chr16	72,095,318	72,095,318

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