A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156153



Internal ID22086658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:43111382..43201367hg38UCSC Ensembl
Outerchr4:43109077..43204398hg38UCSC Ensembl
Innerchr4:43113399..43203384hg19UCSC Ensembl
Outerchr4:43111094..43206415hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3895322
hg1995322
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4014245
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156153
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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