A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv128n21



Internal ID22766320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24446177..24523413hg38UCSC Ensembl
chr14:24915383..24992619hg19UCSC Ensembl
chr14:23985223..24062459hg18UCSC Ensembl
chr14:23985223..24062459hg17UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3877237
hg1977237
hg1877237
hg1777237
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv523200, nsv521915
Samples
Known GenesCMA1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv128n21
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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