A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv839456



Internal ID16133412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30210086..30395361hg38UCSC Ensembl
Innerchr15:30502289..30687564hg19UCSC Ensembl
Innerchr15:28289581..28474856hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38185276
hg19185276
hg18185276
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv568729
Supporting Variants
Samples
Known GenesCHRFAM7A, DKFZP434L187
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv839456
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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