A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv101n21



Internal ID22766293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:115105100..115107151hg38UCSC Ensembl
chr12:115542905..115544956hg19UCSC Ensembl
chr12:114027288..114029339hg18UCSC Ensembl
chr12:114005625..114007676hg17UCSC Ensembl
Cytoband12q24.21
Allele length
AssemblyAllele length
hg382052
hg192052
hg182052
hg172052
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv526565, nsv515549
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv101n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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