A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156142



Internal ID22086647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:35613324..35777869hg38UCSC Ensembl
Outerchr4:35605362..35779183hg38UCSC Ensembl
Innerchr4:35614946..35779491hg19UCSC Ensembl
Outerchr4:35606984..35780805hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38173822
hg19173822
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4014233
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156142
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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