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

dbVar

Database of genomic structural variation

nsv5670715

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 34 studies. See in: genome view

Submitted genomic15,762,129-15,762,129

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5670715	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000021.9	Chr21	15,762,129	15,762,129
nsv5670715	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000021.8	Chr21	17,134,448	17,134,448

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17119228	insertion	SAMN00006466	Sequencing	Sequence alignment	4,625

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17119228	Submitted genomic		NC_000021.9:g.1576 2129_15762130ins10 6	GRCh38 (hg38)		NC_000021.9	Chr21	15,762,129	15,762,129
nssv17119228	Remapped	Perfect	NC_000021.8:g.1713 4448_17134449ins10 6	GRCh37.p13	First Pass	NC_000021.8	Chr21	17,134,448	17,134,448

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