A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6983327



Internal ID12976105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:115631072..115863072hg38UCSC Ensembl
Innerchr11:115501790..115733790hg19UCSC Ensembl
Innerchr11:115007000..115239000hg18UCSC Ensembl
Innerchr11:115007000..115239000hg17UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg38232001
hg19232001
hg18232001
hg17232001
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)essv6983327
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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