A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089622



Internal ID21267266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:77821486..77844128hg38UCSC Ensembl
Innerchr9:80436402..80459044hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg3822643
hg1922643
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110957
Supporting Variants
Samplessample110
Known GenesGNAQ
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089622
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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