A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1025288



Internal ID16319244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:11310662..11312561hg38UCSC Ensembl
Innerchr5:11310774..11312673hg19UCSC Ensembl
Innerchr5:11363774..11365673hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg381900
hg191900
hg181900
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv597147
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)nssv1025288
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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