A curated catalogue of human genomic structural variation




Variant Details

Variant: esv991951



Internal ID6727915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89830059..89832035hg38UCSC Ensembl
Innerchr16:89896467..89898443hg19UCSC Ensembl
Innerchr16:88423968..88425944hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg381977
hg191977
hg181977
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv63e180
Supporting Variantsessv3586977
SamplesHuRef
Known GenesSPIRE2
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv991951
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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