A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25800891



Internal ID18824396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34380017..34408096hg38UCSC Ensembl
Innerchr15:34672218..34700297hg19UCSC Ensembl
Innerchr15:32459510..32487589hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3828080
hg1928080
hg1828080
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892665
Supporting Variants
Samples
Known GenesGOLGA8A, MIR1233-1, MIR1233-2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25800891
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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