A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892288



Internal ID19183108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:18463581..18503037hg38UCSC Ensembl
Outerchr13:18450119..18517755hg38UCSC Ensembl
Innerchr13:19037721..19077177hg19UCSC Ensembl
Outerchr13:19024259..19091895hg19UCSC Ensembl
Innerchr13:17935721..17975177hg18UCSC Ensembl
Outerchr13:17922259..17989895hg18UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg3867637
hg1967637
hg1867637
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792097, essv25792159, essv25790368, essv25791659, essv25791741, essv25792163, essv25789741, essv25791679, essv25791215, essv25792227, essv25792088, essv25792117, essv25791742, essv25791804, essv25792259, essv25792396, essv25792295, essv25792179, essv25792050, essv25792032, essv25791209, essv25791684, essv25792108, essv25789645, essv25789763, essv25792439, essv25792157, essv25791778, essv25789664, essv25791354, essv25789807, essv25792330
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892288
Frequency
Sample Size3017
Observed Gain32
Observed Loss0
Observed Complex0
Frequencyn/a


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