A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1025293



Internal ID16319249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:11384596..11385157hg38UCSC Ensembl
Innerchr5:11384708..11385269hg19UCSC Ensembl
Innerchr5:11437708..11438269hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38562
hg19562
hg18562
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv597151
Supporting Variants
Samples
Known GenesCTNND2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1025293
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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