A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14088821



Internal ID21286543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135414550..135481032hg38UCSC Ensembl
Innerchr9:138306396..138372878hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3866483
hg1966483
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114515
Supporting Variants
Samplessample390
Known GenesPPP1R26, PPP1R26-AS1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14088821
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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