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

dbVar

Database of genomic structural variation

nsv5921587

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:4,847

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: 210 SVs from 42 studies. See in: genome view

Submitted genomic124,499,009-124,503,855

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5921587	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000010.11	Chr10	124,499,009	124,503,855
nsv5921587	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000010.10	Chr10	126,187,578	126,192,424

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17357489	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17357489	Submitted genomic		NC_000010.11:g.124 499009_124503855de l	GRCh38 (hg38)		NC_000010.11	Chr10	124,499,009	124,503,855
nssv17357489	Remapped	Perfect	NC_000010.10:g.126 187578_126192424de l	GRCh37.p13	First Pass	NC_000010.10	Chr10	126,187,578	126,192,424

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