A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv820488



Internal ID15767758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:113206586..113208487hg38UCSC Ensembl
Innerchr13:113860900..113862801hg19UCSC Ensembl
Innerchr13:112908901..112910802hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg381902
hg191902
hg181902
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv563302
Supporting Variants
Samples
Known GenesCUL4A, PCID2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv820488
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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