A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3527924



Internal ID18826205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:66711774..66770368hg38UCSC Ensembl
Innerchr13:67285906..67344500hg19UCSC Ensembl
Innerchr13:66183907..66242501hg18UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg3858595
hg1958595
hg1858595
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1037808
Supporting Variants
Samples
Known GenesPCDH9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3527924
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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