A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv37e55



Internal ID20126516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:133511405..133621047hg38UCSC Ensembl
chr10:135324909..135434551hg19UCSC Ensembl
chr10:135174899..135284541hg18UCSC Ensembl
chr10:135213790..135323432hg17UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38109643
hg19109643
hg18109643
hg17109643
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv34818, esv34810, esv35112, esv35034, esv35006, esv34914, esv34487, esv34721
SamplesNA19171, NA19119, NA19130, NA19128, NA19210, NA19194, NA19154, NA19143
Known GenesCYP2E1, SPRNP1, SYCE1
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)dgv37e55
Frequency
Sample Size771
Observed Gain22
Observed Loss0
Observed Complex0
Frequencyn/a


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