A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6984177



Internal ID12631129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:132953663..133404017hg38UCSC Ensembl
Innerchr11:132823558..133273912hg19UCSC Ensembl
Innerchr11:132328768..132779122hg18UCSC Ensembl
Innerchr11:132328768..132779122hg17UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38450355
hg19450355
hg18450355
hg17450355
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750982
Supporting Variants
SamplesBEC_795
Known GenesOPCML
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6984177
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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