A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3531142



Internal ID18482737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73242046..73278667hg38UCSC Ensembl
Innerchr14:73708754..73745375hg19UCSC Ensembl
Innerchr14:72778507..72815128hg18UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3836622
hg1936622
hg1836622
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042100
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)nssv3531142
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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