A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156042



Internal ID22086547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:164192980..164286863hg38UCSC Ensembl
Outerchr3:164192224..164304130hg38UCSC Ensembl
Innerchr3:163910768..164004651hg19UCSC Ensembl
Outerchr3:163910012..164021918hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38111907
hg19111907
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4016095
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156042
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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