A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6983672



Internal ID12629069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:8410110..8663904hg38UCSC Ensembl
Innerchr11:8431657..8685451hg19UCSC Ensembl
Innerchr11:8388233..8642027hg18UCSC Ensembl
Innerchr11:8388233..8642027hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38253795
hg19253795
hg18253795
hg17253795
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)essv6983672
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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