A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv282n21



Internal ID22766474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:44384499..44420412hg38UCSC Ensembl
chr3:44425991..44461904hg19UCSC Ensembl
chr3:44400995..44436908hg18UCSC Ensembl
chr3:44400995..44436908hg17UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3835914
hg1935914
hg1835914
hg1735914
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv519315, nsv525792
Samples
Known GenesTCAIM
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv282n21
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