A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892665



Internal ID18836799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34380017..34408096hg38UCSC Ensembl
Outerchr15:34380017..34408096hg38UCSC Ensembl
Innerchr15:34672218..34700297hg19UCSC Ensembl
Outerchr15:34672218..34700297hg19UCSC Ensembl
Innerchr15:32459510..32487589hg18UCSC Ensembl
Outerchr15:32459510..32487589hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3828080
hg1928080
hg1828080
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25800891, essv25787096, essv25778380, essv25798947, essv25798634, essv25798890, essv25798906, essv25799220, essv25784801
Samples
Known GenesGOLGA8A, MIR1233-1, MIR1233-2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892665
Frequency
Sample Size3017
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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