A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7468913



Internal ID10400509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:23899566..23899872hg38UCSC Ensembl
Outerchr16:23910887..23911193hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3199346
Supporting Variants
SamplesHuRef
Known GenesPRKCB
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)essv7468913
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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