A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6988248



Internal ID12980790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:81652086..81718326hg38UCSC Ensembl
Innerchr11:81363128..81429368hg19UCSC Ensembl
Innerchr11:81040776..81107016hg18UCSC Ensembl
Innerchr11:81040776..81107016hg17UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3866241
hg1966241
hg1866241
hg1766241
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)essv6988248
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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