A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv113n21



Internal ID22766305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:74376396..74409017hg38UCSC Ensembl
chr13:74950533..74983154hg19UCSC Ensembl
chr13:73848534..73881155hg18UCSC Ensembl
chr13:73848534..73881155hg17UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg3832622
hg1932622
hg1832622
hg1732622
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv520870, nsv527787
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv113n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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