A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1220n54



Internal ID22769115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:65662026..65714631hg38UCSC Ensembl
chr10:67421784..67474389hg19UCSC Ensembl
chr10:67091790..67144395hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3852606
hg1952606
hg1852606
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv551291, nsv551289, nsv551292, nsv551290
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1220n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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