A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1239n106



Internal ID22795067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72644259..72660759hg38UCSC Ensembl
chr15:72936600..72953100hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3816501
hg1916501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1110258, nsv1141266
SamplesKWS2, KWS1
Known GenesGOLGA6B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1239n106
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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