A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14090867



Internal ID21275045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:81885419..81912738hg38UCSC Ensembl
Innerchr9:84500334..84527653hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3827320
hg1927320
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113733
Supporting Variants
Samplessample216
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14090867
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer