A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14088010



Internal ID21279914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133065120..133090666hg38UCSC Ensembl
Innerchr9:135940507..135966053hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3825547
hg1925547
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117195
Supporting Variants
Samplessample290
Known GenesCEL, CELP
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14088010
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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