A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037808



Internal ID19127027
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 StatusM
Merged Variantsdgv1700n100
Supporting Variantsnssv3527924
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)nsv1037808
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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