A curated catalogue of human genomic structural variation




Variant Details

Variant: esv994657



Internal ID7079192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28584069..28665552hg38UCSC Ensembl
Innerchr15:28829215..28910698hg19UCSC Ensembl
Innerchr15:26628256..26709739hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3881484
hg1981484
hg1881484
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586178
SamplesHuRef
Known GenesHERC2P9
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv994657
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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