A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3713529



Internal ID18665124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:77411078..77470626hg38UCSC Ensembl
Innerchr14:77877421..77936969hg19UCSC Ensembl
Innerchr14:76947174..77006722hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3859549
hg1959549
hg1859549
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1041985
Supporting Variants
Samples
Known GenesAHSA1, NOXRED1, VIPAS39
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3713529
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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