A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155885



Internal ID22086390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:177741042..177756795hg38UCSC Ensembl
Outerchr2:177739418..177756982hg38UCSC Ensembl
Innerchr2:178605770..178621523hg19UCSC Ensembl
Outerchr2:178604146..178621710hg19UCSC Ensembl
Cytoband2q31.2
Allele length
AssemblyAllele length
hg3817565
hg1917565
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4015309
Samples
Known GenesPDE11A
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155885
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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