A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788255



Internal ID18818071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133438843..133527063hg38UCSC Ensembl
Innerchr10:135252347..135340567hg19UCSC Ensembl
Innerchr10:135102337..135190557hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3888221
hg1988221
hg1888221
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891902
Supporting Variants
Samples
Known GenesSCART1
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=28
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788255
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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