A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv100n21



Internal ID22766292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:114531958..114568632hg38UCSC Ensembl
chr12:114969763..115006437hg19UCSC Ensembl
chr12:113454146..113490820hg18UCSC Ensembl
chr12:113432483..113469157hg17UCSC Ensembl
Cytoband12q24.21
Allele length
AssemblyAllele length
hg3836675
hg1936675
hg1836675
hg1736675
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv521912, nsv522051
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv100n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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