A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4017910



Internal ID22079541
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 Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156086
Supporting Variants
Samples
Known GenesPKN2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4017910
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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