A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3504578



Internal ID18456173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:76160196..76193582hg38UCSC Ensembl
Innerchr11:75871240..75904626hg19UCSC Ensembl
Innerchr11:75548888..75582274hg18UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg3833387
hg1933387
hg1833387
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1053580
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)nssv3504578
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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