A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116775



Internal ID21300041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:79301553..79302652hg38UCSC Ensembl
Innerchr9:81916468..81917567hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14090763
Samplessample166
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116775
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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