A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787912



Internal ID19182126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:22774022..22824912hg38UCSC Ensembl
Innerchr10:23062951..23113841hg19UCSC Ensembl
Innerchr10:23102957..23153847hg18UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg3850891
hg1950891
hg1850891
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891776
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=11
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787912
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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