A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3531146



Internal ID18482741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73250066..73273941hg38UCSC Ensembl
Innerchr14:73716774..73740649hg19UCSC Ensembl
Innerchr14:72786527..72810402hg18UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3823876
hg1923876
hg1823876
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1037814
Supporting Variants
Samples
Known GenesPAPLN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3531146
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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