A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586977



Internal ID6711673
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 OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv991951
Supporting Variants
SamplesHuRef
Known GenesSPIRE2
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586977
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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