A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894164



Internal ID19185233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:29351106..29569068hg38UCSC Ensembl
Outerchr5:29327804..29574668hg38UCSC Ensembl
Innerchr5:29351213..29569175hg19UCSC Ensembl
Outerchr5:29327911..29574775hg19UCSC Ensembl
Innerchr5:29386970..29604932hg18UCSC Ensembl
Outerchr5:29363668..29610532hg18UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg38246865
hg19246865
hg18246865
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789739, essv25788623, essv25791971, essv25791257, essv25792605, essv25788901, essv25789541, essv25788607, essv25791122
Samples
Known GenesLOC101929681
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894164
Frequency
Sample Size3017
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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