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

dbVar

Database of genomic structural variation

nsv5922613

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:538

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

Submitted genomic132,440,211-132,440,748

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5922613	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000010.11	Chr10	132,440,211	132,440,748
nsv5922613	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000010.10	Chr10	134,253,715	134,254,252

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17350884	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17350884	Submitted genomic		NC_000010.11:g.132 440211_132440748de l	GRCh38 (hg38)		NC_000010.11	Chr10	132,440,211	132,440,748
nssv17350884	Remapped	Perfect	NC_000010.10:g.134 253715_134254252de l	GRCh37.p13	First Pass	NC_000010.10	Chr10	134,253,715	134,254,252

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