A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1158n106



Internal ID19019267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20810471..20835771hg38UCSC Ensembl
chr15:21015800..21041100hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3825301
hg1925301
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1139614, nsv1128710
SamplesKWS1, KWS2
Known GenesPOTEB, POTEB2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1158n106
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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