A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156086



Internal ID22086591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:88799948..88837543hg38UCSC Ensembl
Outerchr1:88794408..88842283hg38UCSC Ensembl
Innerchr1:89265631..89303226hg19UCSC Ensembl
Outerchr1:89260091..89307966hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg3847876
hg1947876
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11n97
Supporting Variantsnssv4017910
Samples
Known GenesPKN2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156086
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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