A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987432



Internal ID12629325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:132980840..133396436hg38UCSC Ensembl
Innerchr11:132850735..133266331hg19UCSC Ensembl
Innerchr11:132355945..132771541hg18UCSC Ensembl
Innerchr11:132355945..132771541hg17UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38415597
hg19415597
hg18415597
hg17415597
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 Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6987432
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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