A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563166



Internal ID16350575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:111024573..111096769hg38UCSC Ensembl
Innerchr13:111676920..111749116hg19UCSC Ensembl
Innerchr13:110474921..110547117hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3872197
hg1972197
hg1872197
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3405n54
Supporting Variantsnssv819923
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563166
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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