A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891744



Internal ID18839454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5269112..5354365hg38UCSC Ensembl
Outerchr10:5230815..5366498hg38UCSC Ensembl
Innerchr10:5311075..5396328hg19UCSC Ensembl
Outerchr10:5272778..5408461hg19UCSC Ensembl
Innerchr10:5301075..5386328hg18UCSC Ensembl
Outerchr10:5262778..5398461hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38135684
hg19135684
hg18135684
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788210, essv25788153, essv25792966, essv25788145
Samples
Known GenesUCN3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891744
Frequency
Sample Size3017
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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