A curated catalogue of human genomic structural variation




Variant Details

Variant: essv2585877



Internal ID770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:12315765..12315776hg38UCSC Ensembl
Outerchr11:12308374..12317250hg38UCSC Ensembl
Innerchr11:12337312..12337323hg19UCSC Ensembl
Outerchr11:12329921..12338797hg19UCSC Ensembl
Innerchr11:12293888..12293899hg18UCSC Ensembl
Outerchr11:12286497..12295373hg18UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg388877
hg198877
hg188877
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv275255
Supporting Variants
Samples
Known GenesMICALCL
MethodSNP array
AnalysisIdentification of germline Changes in Copy Number (IgC2N)
PlatformAffymetrix SNP 6.0
Comments
ReferenceBanerjee_et_al_2011
Pubmed ID21479260
Accession Number(s)essv2585877
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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