A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894163



Internal ID19185232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:29351779..29433992hg38UCSC Ensembl
Outerchr5:29313335..29440324hg38UCSC Ensembl
Innerchr5:29351886..29434099hg19UCSC Ensembl
Outerchr5:29313442..29440431hg19UCSC Ensembl
Innerchr5:29387643..29469856hg18UCSC Ensembl
Outerchr5:29349199..29476188hg18UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg38126990
hg19126990
hg18126990
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787801, essv25788747, essv25789411, essv25788306, essv25787788, essv25788029, essv25788303
Samples
Known GenesLOC101929681
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894163
Frequency
Sample Size3017
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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