A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562979



Internal ID16350388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:102466643..102489183hg38UCSC Ensembl
Innerchr13:103118993..103141533hg19UCSC Ensembl
Innerchr13:101916994..101939534hg18UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3822541
hg1922541
hg1822541
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv818819
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562979
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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