A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv121n21



Internal ID22766313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113971527..114164720hg38UCSC Ensembl
chr13:114740938..114930195hg19UCSC Ensembl
chr13:113759040..113948297hg18UCSC Ensembl
chr13:113759040..113948297hg17UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38193194
hg19189258
hg18189258
hg17189258
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv527299, nsv524254
Samples
Known GenesRASA3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv121n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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