A curated catalogue of human genomic structural variation




Variant Details

Variant: esv997919



Internal ID6733859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70101646..70164038hg38UCSC Ensembl
Innerchr16:70135549..70197941hg19UCSC Ensembl
Innerchr16:68693050..68755442hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3862393
hg1962393
hg1862393
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586813
SamplesHuRef
Known GenesPDPR
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv997919
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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