A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979234



Internal ID12633157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15666599..15698940hg38UCSC Ensembl
Innerchr19:15777409..15809750hg19UCSC Ensembl
Innerchr19:15638409..15670750hg18UCSC Ensembl
Innerchr19:15638409..15670750hg17UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3832342
hg1932342
hg1832342
hg1732342
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34445
Supporting Variants
SamplesNA18515
Known GenesCYP4F12
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979234
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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