A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv883n100



Internal ID22786970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:65534804..65568671hg38UCSC Ensembl
chr10:67294562..67328429hg19UCSC Ensembl
chr10:66964568..66998435hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3833868
hg1933868
hg1833868
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1037854, nsv1050080, nsv1039988, nsv1053606, nsv1035778
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv883n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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