A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6983826



Internal ID12629317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:132954476..133379054hg38UCSC Ensembl
Innerchr11:132824371..133248949hg19UCSC Ensembl
Innerchr11:132329581..132754159hg18UCSC Ensembl
Innerchr11:132329581..132754159hg17UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38424579
hg19424579
hg18424579
hg17424579
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750983
Supporting Variants
SamplesBEC_631
Known GenesOPCML
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6983826
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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