A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4015309



Internal ID22076940
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 Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155885
Supporting Variants
Samples
Known GenesPDE11A
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4015309
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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