A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17699566



Internal ID123232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:26751569..26751894hg38UCSC Ensembl
chr15:26996716..26997041hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5495059
Supporting Variants
Samples
Known GenesGABRB3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17699566
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001249


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer