A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6988656



Internal ID12976110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:115631076..115863329hg38UCSC Ensembl
Innerchr11:115501794..115734047hg19UCSC Ensembl
Innerchr11:115007004..115239257hg18UCSC Ensembl
Innerchr11:115007004..115239257hg17UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg38232254
hg19232254
hg18232254
hg17232254
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750981
Supporting Variants
SamplesBEC_639
Known GenesLINC00900
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6988656
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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