A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14088140



Internal ID21284360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:29616405..29631561hg38UCSC Ensembl
Innerchr9:29616403..29631559hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3815157
hg1915157
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111072
Supporting Variants
Samplessample360
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14088140
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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