A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv116n21



Internal ID20131837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:90734186..90746498hg38UCSC Ensembl
chr13:91386440..91398752hg19UCSC Ensembl
chr13:90184441..90196753hg18UCSC Ensembl
chr13:90184441..90196753hg17UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3812313
hg1912313
hg1812313
hg1712313
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv526357, nsv521546
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv116n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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