A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116793



Internal ID21300059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:1656054..1717393hg38UCSC Ensembl
Innerchr1:1587504..1648832hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3861340
hg1961329
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14092243
Samplessample120
Known GenesCDK11A, CDK11B, MMP23A, SLC35E2B
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116793
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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