A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788134



Internal ID19171038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:64613740..65058252hg38UCSC Ensembl
Innerchr10:66373497..66818010hg19UCSC Ensembl
Innerchr10:66043503..66488016hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38444513
hg19444514
hg18444514
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=69
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788134
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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