A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156085



Internal ID22086590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:88799948..88834486hg38UCSC Ensembl
Outerchr1:88794408..88837272hg38UCSC Ensembl
Innerchr1:89265631..89300169hg19UCSC Ensembl
Outerchr1:89260091..89302955hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg3842865
hg1942865
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11n97
Supporting Variantsnssv4017907, nssv4017909
Samples
Known GenesPKN2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156085
Frequency
Sample Size131
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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