A curated catalogue of human genomic structural variation




Variant Details

Variant: esv989873



Internal ID7061116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81866391..81866674hg38UCSC Ensembl
chr16:81899996..81900279hg19UCSC Ensembl
chr16:80457497..80457780hg18UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg38284
hg19284
hg18284
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3574765
SamplesHuRef
Known GenesPLCG2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv989873
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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