A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4019398



Internal ID22081029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:177622954..177675376hg38UCSC Ensembl
Outerchr4:177617307..177675391hg38UCSC Ensembl
Innerchr4:178544108..178596530hg19UCSC Ensembl
Outerchr4:178538461..178596545hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg3858085
hg1958085
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156275
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4019398
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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