A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3531141



Internal ID18482736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73242046..73276659hg38UCSC Ensembl
Innerchr14:73708754..73743367hg19UCSC Ensembl
Innerchr14:72778507..72813120hg18UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3834614
hg1934614
hg1834614
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048542
Supporting Variants
Samples
Known GenesNUMB, PAPLN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3531141
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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