A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4014236



Internal ID22075867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:35952943..35997032hg38UCSC Ensembl
Outerchr4:35950052..35999241hg38UCSC Ensembl
Innerchr4:35954565..35998654hg19UCSC Ensembl
Outerchr4:35951674..36000863hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3849190
hg1949190
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156145
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4014236
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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