A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3377n54



Internal ID22771272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:108078533..108111109hg38UCSC Ensembl
chr13:108730881..108763457hg19UCSC Ensembl
chr13:107528882..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 Variants
Supporting Variantsnsv563023, nsv563022
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3377n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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