A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3713507



Internal ID18665102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:63310406..63390818hg38UCSC Ensembl
Innerchr14:63777124..63857536hg19UCSC Ensembl
Innerchr14:62846877..62927289hg18UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg3880413
hg1980413
hg1880413
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1045700
Supporting Variants
Samples
Known GenesGPHB5, PPP2R5E
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3713507
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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