A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562259



Internal ID16349668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:71307506..71369911hg38UCSC Ensembl
Innerchr13:71881638..71944043hg19UCSC Ensembl
Innerchr13:70779639..70842044hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3862406
hg1962406
hg1862406
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3240n54
Supporting Variantsnssv813806
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562259
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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