A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1147434



Internal ID18855495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:46745601..46747102hg38UCSC Ensembl
Outerchr15:47037799..47039300hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg381502
hg191502
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4000210
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1147434
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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