A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1025292



Internal ID16319248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:11384596..11385085hg38UCSC Ensembl
Innerchr5:11384708..11385197hg19UCSC Ensembl
Innerchr5:11437708..11438197hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38490
hg19490
hg18490
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv597150
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)nssv1025292
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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