A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892664



Internal ID18836798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34408096..34496365hg38UCSC Ensembl
Outerchr15:34380017..34546808hg38UCSC Ensembl
Innerchr15:34700297..34788566hg19UCSC Ensembl
Outerchr15:34672218..34839009hg19UCSC Ensembl
Innerchr15:32487589..32575858hg18UCSC Ensembl
Outerchr15:32459510..32626301hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38166792
hg19166792
hg18166792
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25798129, essv25793022, essv25782823, essv25782763, essv25788758, essv25782956, essv25787443, essv25799182, essv25788886, essv25788972, essv25798120, essv25793119, essv25790735, essv25799778, essv25788883, essv25790261, essv25800581, essv25785670, essv25789482, essv25798997, essv25779589
Samples
Known GenesGOLGA8A, GOLGA8B, MIR1233-1, MIR1233-2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892664
Frequency
Sample Size3017
Observed Gain9
Observed Loss12
Observed Complex0
Frequencyn/a


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