A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989839



Internal ID12629063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:8410107..8622437hg38UCSC Ensembl
Innerchr11:8431654..8643984hg19UCSC Ensembl
Innerchr11:8388230..8600560hg18UCSC Ensembl
Innerchr11:8388230..8600560hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38212331
hg19212331
hg18212331
hg17212331
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751035
Supporting Variants
SamplesBEC_611
Known GenesSTK33, TRIM66
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6989839
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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