A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4011100



Internal ID22072731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:59388850..59418381hg38UCSC Ensembl
Outerchr15:59386574..59418538hg38UCSC Ensembl
Innerchr15:59681049..59710580hg19UCSC Ensembl
Outerchr15:59678773..59710737hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3831965
hg1931965
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155183
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4011100
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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