A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1213n54



Internal ID22769108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:65120965..65178823hg38UCSC Ensembl
chr10:66880723..66938581hg19UCSC Ensembl
chr10:66550729..66608587hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3857859
hg1957859
hg1857859
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv551236, nsv551238, nsv551237
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1213n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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