A curated catalogue of human genomic structural variation




Variant Details

Variant: esv993231



Internal ID6729192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83087151..83087763hg38UCSC Ensembl
Innerchr16:83120756..83121368hg19UCSC Ensembl
Innerchr16:81678257..81678869hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg38613
hg19613
hg18613
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3587203
SamplesHuRef
Known GenesCDH13
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv993231
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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