A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv840042



Internal ID15787312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34430024..34470157hg38UCSC Ensembl
Innerchr15:34722225..34762358hg19UCSC Ensembl
Innerchr15:32509517..32549650hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3840134
hg1940134
hg1840134
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569011
Supporting Variants
Samples
Known GenesGOLGA8A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv840042
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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