A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562138



Internal ID16349547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:66881655..66937298hg38UCSC Ensembl
Innerchr13:67455787..67511430hg19UCSC Ensembl
Innerchr13:66353788..66409431hg18UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg3855644
hg1955644
hg1855644
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv813411
Samples
Known GenesPCDH9, PCDH9-AS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562138
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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