A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3511450



Internal ID18809731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:76161714..76211868hg38UCSC Ensembl
Innerchr11:75872758..75922912hg19UCSC Ensembl
Innerchr11:75550406..75600560hg18UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg3850155
hg1950155
hg1850155
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044943
Supporting Variants
Samples
Known GenesWNT11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3511450
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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