A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3514794



Internal ID18466389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:198560..270715hg38UCSC Ensembl
Innerchr11:198560..270715hg19UCSC Ensembl
Innerchr11:188560..260715hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3872156
hg1972156
hg1872156
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043090
Supporting Variants
Samples
Known GenesBET1L, MIR6743, ODF3, PSMD13, RIC8A, SIRT3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3514794
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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