A curated catalogue of human genomic structural variation




Variant Details

Variant: esv997589



Internal ID6733531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:23899565..23899870hg38UCSC Ensembl
chr16:23910886..23911191hg19UCSC Ensembl
chr16:23818387..23818692hg18UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38306
hg19306
hg18306
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3584459
SamplesHuRef
Known GenesPRKCB
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv997589
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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