A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156056



Internal ID22086561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:179903538..179963848hg38UCSC Ensembl
Outerchr3:179900467..179969450hg38UCSC Ensembl
Innerchr3:179621326..179681636hg19UCSC Ensembl
Outerchr3:179618255..179687238hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg3868984
hg1968984
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4017220
Samples
Known GenesPEX5L
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156056
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer