A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv137e55



Internal ID20126616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15666599..15728649hg38UCSC Ensembl
chr19:15777409..15839459hg19UCSC Ensembl
chr19:15638409..15700459hg18UCSC Ensembl
chr19:15638409..15700459hg17UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3862051
hg1962051
hg1862051
hg1762051
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv34923, esv34718, esv34445, esv34310, esv34230, esv35069, esv34422, esv34334
SamplesNA19171, NA18860, NA18859, NA18515, NA18523, NA19173, NA18854, NA18505
Known GenesCYP4F12, OR10H2
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)dgv137e55
Frequency
Sample Size771
Observed Gain20
Observed Loss0
Observed Complex0
Frequencyn/a


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