A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3182679



Internal ID10855659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:88933336..88933777hg38UCSC Ensembl
Outerchr16:88999744..89000185hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38442
hg19442
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7452246
SamplesHuRef
Known GenesCBFA2T3
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)esv3182679
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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