A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156156



Internal ID22086661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:43739854..43829201hg38UCSC Ensembl
Outerchr4:43739613..43830154hg38UCSC Ensembl
Innerchr4:43741871..43831218hg19UCSC Ensembl
Outerchr4:43741630..43832171hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3890542
hg1990542
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4014248
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156156
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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