A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6980994



Internal ID12635719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15669190..15698990hg38UCSC Ensembl
Innerchr19:15780000..15809800hg19UCSC Ensembl
Innerchr19:15641000..15670800hg18UCSC Ensembl
Innerchr19:15641000..15670800hg17UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3829801
hg1929801
hg1829801
hg1729801
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35069
Supporting Variants
SamplesNA19171
Known GenesCYP4F12
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6980994
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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