A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586355



Internal ID7057737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20344141..20504928hg38UCSC Ensembl
Innerchr15:20549394..20710181hg19UCSC Ensembl
Innerchr15:18809408..18970195hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38160788
hg19160788
hg18160788
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv998961
Supporting Variants
SamplesHuRef
Known GenesHERC2P3
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586355
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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