A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4016332



Internal ID22077963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:26392633..26397852hg38UCSC Ensembl
Outerchr3:26384700..26404482hg38UCSC Ensembl
Innerchr3:26434124..26439343hg19UCSC Ensembl
Outerchr3:26426191..26445973hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3819783
hg1919783
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155955
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4016332
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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