A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv840264



Internal ID15787534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34438557..34579095hg38UCSC Ensembl
Innerchr15:34730758..34871296hg19UCSC Ensembl
Innerchr15:32518050..32658588hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38140539
hg19140539
hg18140539
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569068
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)nssv840264
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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