A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089588



Internal ID21292804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:14863507..14887037hg38UCSC Ensembl
Innerchr9:14863505..14887035hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3823531
hg1923531
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114852
Supporting Variants
Samplessample91
Known GenesFREM1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089588
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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