A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3514934



Internal ID18466529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:132954183..133396436hg38UCSC Ensembl
Innerchr11:132824078..133266331hg19UCSC Ensembl
Innerchr11:132329288..132771541hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38442254
hg19442254
hg18442254
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1038734
Supporting Variants
Samples
Known GenesOPCML
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3514934
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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