A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089740



Internal ID21270825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:92360248..92424306hg38UCSC Ensembl
Innerchr9:95122530..95186588hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3864059
hg1964059
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3118343
Supporting Variants
Samplessample155
Known GenesCENPP, OGN, OMD
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089740
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