A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1934n100



Internal ID20153550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73248673..73278667hg38UCSC Ensembl
chr14:73715381..73745375hg19UCSC Ensembl
chr14:72785134..72815128hg18UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3829995
hg1929995
hg1829995
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1044356, nsv1035179, nsv1037814, nsv1038445
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)dgv1934n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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