A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25791421



Internal ID18836169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:7598031..7693943hg38UCSC Ensembl
Innerchr11:7619262..7715174hg19UCSC Ensembl
Innerchr11:7575838..7671750hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3895913
hg1995913
hg1895913
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891925
Supporting Variants
Samples
Known GenesCYB5R2, OVCH2, PPFIBP2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=52
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25791421
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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