A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6985523



Internal ID12626387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12040126..12286403hg17UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg17246278
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752199
Supporting Variants
SamplesBEC_375
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6985523
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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