A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597145



Internal ID16384554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:11275173..11292982hg38UCSC Ensembl
Innerchr5:11275285..11293094hg19UCSC Ensembl
Innerchr5:11328285..11346094hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3817810
hg1917810
hg1817810
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1025286
Samples
Known GenesCTNND2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597145
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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