A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6984178



Internal ID12631124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:132980895..133396894hg38UCSC Ensembl
Innerchr11:132850790..133266789hg19UCSC Ensembl
Innerchr11:132356000..132771999hg18UCSC Ensembl
Innerchr11:132356000..132771999hg17UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38416000
hg19416000
hg18416000
hg17416000
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 Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6984178
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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