A curated catalogue of human genomic structural variation




Variant Details

Variant: essv2585139



Internal ID346718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:86497292..86497861hg38UCSC Ensembl
Outerchr11:86495988..86498514hg38UCSC Ensembl
Innerchr11:86208334..86208903hg19UCSC Ensembl
Outerchr11:86207030..86209556hg19UCSC Ensembl
Innerchr11:85885982..85886551hg18UCSC Ensembl
Outerchr11:85884678..85887204hg18UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg382527
hg192527
hg182527
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv274960
Supporting Variants
Samples
Known GenesME3
MethodSNP array
AnalysisIdentification of germline Changes in Copy Number (IgC2N)
PlatformAffymetrix SNP 6.0
Comments
ReferenceBanerjee_et_al_2011
Pubmed ID21479260
Accession Number(s)essv2585139
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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