A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4015852



Internal ID22077483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:132273929..132276840hg38UCSC Ensembl
Outerchr3:132273893..132281633hg38UCSC Ensembl
Innerchr3:131992773..131995684hg19UCSC Ensembl
Outerchr3:131992737..132000477hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg387741
hg197741
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156019
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4015852
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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