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

dbVar

Database of genomic structural variation

nsv5918822

Organism: Homo sapiens

Study:nstd209 (Almarri et al. 2020)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:2,973

Publication(s):Almarri et al. 2020

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: 184 SVs from 44 studies. See in: genome view

Submitted genomic123,183,917-123,186,889

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5918822	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	123,183,917	123,186,889
nsv5918822	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	122,823,971	122,826,943

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17445116	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17445116	Submitted genomic		NC_000007.14:g.123 183917_123186889de l	GRCh38 (hg38)		NC_000007.14	Chr7	123,183,917	123,186,889
nssv17445116	Remapped	Perfect	NC_000007.13:g.122 823971_122826943de l	GRCh37.p13	First Pass	NC_000007.13	Chr7	122,823,971	122,826,943

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