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

dbVar

Database of genomic structural variation

nsv5829361

Organism: Homo sapiens

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

Variant Calls:2
Validation:Not tested
Clinical Assertions: No
Region Size:11,278

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: 203 SVs from 56 studies. See in: genome view

Submitted genomic21,967,929-21,979,206

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5829361	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000001.11	Chr1	21,967,929	21,979,206
nsv5829361	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	22,294,422	22,305,699

Variant Call Information

Variant Call ID	Type	Method	Analysis	Copy number
nssv17453888	copy number variation	Sequencing	Sequence alignment	2
nssv17469081	copy number variation	Sequencing	Sequence alignment	0

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17453888	Submitted genomic		GRCh38 (hg38)		NC_000001.11	Chr1	21,967,929	21,979,206
nssv17469081	Submitted genomic		GRCh38 (hg38)		NC_000001.11	Chr1	21,967,929	21,979,206
nssv17453888	Remapped	Perfect	GRCh37.p13	First Pass	NC_000001.10	Chr1	22,294,422	22,305,699
nssv17469081	Remapped	Perfect	GRCh37.p13	First Pass	NC_000001.10	Chr1	22,294,422	22,305,699

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