A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1278n106



Internal ID22795106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:101892697..101979797hg38UCSC Ensembl
chr15:102432900..102520000hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3887101
hg1987101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1139640, nsv1128729
SamplesKWS2, KWS1
Known GenesDDX11L9, FAM138E, MIR6859-1, MIR6859-2, OR4F4, WASH3P
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1278n106
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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