A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv839854



Internal ID15787124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34413285..34558792hg38UCSC Ensembl
Innerchr15:34705486..34850993hg19UCSC Ensembl
Innerchr15:32492778..32638285hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38145508
hg19145508
hg18145508
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv568968
Supporting Variants
Samples
Known GenesGOLGA8A, GOLGA8B, MIR1233-1, MIR1233-2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv839854
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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