A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1326n106



Internal ID20160683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24115187..24115409hg38UCSC Ensembl
chr16:24126508..24126730hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38223
hg19223
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1111939, nsv1135036
SamplesKWS2
Known GenesPRKCB
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1326n106
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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