A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4008164



Internal ID22069795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:66656559..66707495hg38UCSC Ensembl
Outerchr13:66645983..66711786hg38UCSC Ensembl
Innerchr13:67230691..67281627hg19UCSC Ensembl
Outerchr13:67220115..67285918hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg3865804
hg1965804
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154926
Supporting Variants
Samples
Known GenesPCDH9
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4008164
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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