A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788183



Internal ID19165174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:64611972..65067872hg38UCSC Ensembl
Innerchr10:66371729..66827630hg19UCSC Ensembl
Innerchr10:66041735..66497636hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38455901
hg19455902
hg18455902
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891832
Supporting Variants
Samples
Known GenesANXA2P3
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=68
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788183
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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