A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4366n100



Internal ID22790453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:10502083..10558343hg38UCSC Ensembl
chr21:10954114..11010374hg19UCSC Ensembl
chr21:9975985..10032245hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg3856261
hg1956261
hg1856261
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1057432, nsv1058888, nsv1057768
Samples
Known GenesTPTE
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4366n100
Frequency
Sample Size11257
Observed Gain6
Observed Loss15
Observed Complex0
Frequencyn/a


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