A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv264n21



Internal ID22766456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:47275457..47291868hg38UCSC Ensembl
chr22:47671207..47687618hg19UCSC Ensembl
chr22:46049871..46066282hg18UCSC Ensembl
chr22:45991726..46008137hg17UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3816412
hg1916412
hg1816412
hg1716412
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv526738, nsv522864
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv264n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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