A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044356



Internal ID18786887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73250066..73278667hg38UCSC Ensembl
Innerchr14:73716774..73745375hg19UCSC Ensembl
Innerchr14:72786527..72815128hg18UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3828602
hg1928602
hg1828602
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1934n100
Supporting Variantsnssv3531150
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)nsv1044356
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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