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

dbVar

Database of genomic structural variation

nsv5942882

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:3,199

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: 227 SVs from 23 studies. See in: genome view

Submitted genomic99,195,980-99,199,178

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5942882	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000013.11	Chr13	99,195,980	99,199,178
nsv5942882	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000013.10	Chr13	99,848,234	99,851,432

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17384213	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17384213	Submitted genomic		NC_000013.11:g.991 95980_99199178del	GRCh38 (hg38)		NC_000013.11	Chr13	99,195,980	99,199,178
nssv17384213	Remapped	Perfect	NC_000013.10:g.998 48234_99851432del	GRCh37.p13	First Pass	NC_000013.10	Chr13	99,848,234	99,851,432

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