A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1141266



Internal ID19281787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:72644259..72660759hg38UCSC Ensembl
Outerchr15:72936600..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 Variantsdgv1239n106
Supporting Variantsnssv3992771
SamplesKWS2
Known GenesGOLGA6B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1141266
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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