A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089602



Internal ID21293297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:95504976..95510557hg38UCSC Ensembl
Innerchr9:98267258..98272839hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg385582
hg195582
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114675
Supporting Variants
Samplessample98
Known GenesPTCH1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089602
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