A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv51e55



Internal ID22761001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:55677818..55853223hg38UCSC Ensembl
chr11:55445294..55620699hg19UCSC Ensembl
chr11:55201870..55377275hg18UCSC Ensembl
chr11:55201870..55377275hg17UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38175406
hg19175406
hg18175406
hg17175406
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv34812, esv35147, esv34760, esv35012, esv34561
SamplesNA19239, NA19209, NA19094, NA18854, NA18852
Known GenesOR5D13, OR5D14, OR5D16, OR5D18, OR5L1, OR5L2
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Affymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)dgv51e55
Frequency
Sample Size771
Observed Gain0
Observed Loss22
Observed Complex0
Frequencyn/a


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