A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3n21



Internal ID22766195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28781383..28818676hg38UCSC Ensembl
chr1:29107895..29145188hg19UCSC Ensembl
chr1:28980482..29017775hg18UCSC Ensembl
chr1:28928511..28965804hg17UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg3837294
hg1937294
hg1837294
hg1737294
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv517547, nsv525553
Samples
Known GenesOPRD1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv3n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer