A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3533551



Internal ID18831832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:101067588..101088705hg38UCSC Ensembl
Innerchr14:101533925..101555042hg19UCSC Ensembl
Innerchr14:100603678..100624795hg18UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3821118
hg1921118
hg1821118
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1041303
Supporting Variants
Samples
Known GenesMEG9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3533551
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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