A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1118n54



Internal ID18993294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46287904..46332377hg38UCSC Ensembl
chr10:47659140..47703613hg19UCSC Ensembl
chr10:47129146..47173619hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3844474
hg1944474
hg1844474
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv550796, nsv550797
SamplesHGDP01401, HGDP00919, HGDP00743, HGDP01384
Known GenesANTXRL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1118n54
Frequency
Sample Size17421
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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