A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1325n106



Internal ID20160682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:23899550..23899871hg38UCSC Ensembl
chr16:23910871..23911192hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1142752, nsv1112017
SamplesKWS1
Known GenesPRKCB
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1325n106
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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