A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv306n21



Internal ID22766498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:182356115..182441639hg38UCSC Ensembl
chr3:182073903..182159427hg19UCSC Ensembl
chr3:183556597..183642121hg18UCSC Ensembl
chr3:183556605..183642129hg17UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg3885525
hg1985525
hg1885525
hg1785525
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv522175, nsv519493
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv306n21
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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