A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989121



Internal ID12980795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:81652110..81718310hg38UCSC Ensembl
Innerchr11:81363152..81429352hg19UCSC Ensembl
Innerchr11:81040800..81107000hg18UCSC Ensembl
Innerchr11:81040800..81107000hg17UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3866201
hg1966201
hg1866201
hg1766201
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34835
Supporting Variants
SamplesNA18633
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6989121
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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