A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788240



Internal ID18822766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:12196611..12327861hg38UCSC Ensembl
Innerchr10:12238610..12369860hg19UCSC Ensembl
Innerchr10:12278616..12409866hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38131251
hg19131251
hg18131251
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891757
Supporting Variants
Samples
Known GenesCDC123
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=42
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788240
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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