A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042182



Internal ID18784713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:72582998..72637447hg38UCSC Ensembl
Innerchr11:72294042..72348491hg19UCSC Ensembl
Innerchr11:71971690..72026139hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3854450
hg1954450
hg1854450
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3506455
Samples
Known GenesMIR139, PDE2A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042182
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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