A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1333n106



Internal ID20160690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:27324879..27339881hg38UCSC Ensembl
chr16:27336200..27351202hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3815003
hg1915003
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1111791, nsv1121163
SamplesKWS2
Known GenesIL4R
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1333n106
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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