A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563023



Internal ID16350432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:108078533..108111109hg38UCSC Ensembl
Innerchr13:108730881..108763457hg19UCSC Ensembl
Innerchr13:107528882..107561458hg18UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3832577
hg1932577
hg1832577
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3377n54
Supporting Variantsnssv819259
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563023
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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