A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv840232



Internal ID15787502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34438557..34545691hg38UCSC Ensembl
Innerchr15:34730758..34837892hg19UCSC Ensembl
Innerchr15:32518050..32625184hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38107135
hg19107135
hg18107135
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569065
Supporting Variants
Samples
Known GenesGOLGA8B, MIR1233-1, MIR1233-2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv840232
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