A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563095



Internal ID16350504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:110072363..110109174hg38UCSC Ensembl
Innerchr13:110724710..110761521hg19UCSC Ensembl
Innerchr13:109522711..109559522hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3836812
hg1936812
hg1836812
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv819725
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563095
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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