A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1109n54



Internal ID20134533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46166132..46332633hg38UCSC Ensembl
chr10:47537368..47703869hg19UCSC Ensembl
chr10:47007374..47173875hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38166502
hg19166502
hg18166502
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv550765, nsv550748, nsv550752, nsv550749, nsv550754, nsv550753, nsv550756, nsv550767, nsv550766, nsv550733, nsv550734, nsv550750
SamplesHGDP00157, HGDP01379, 1780862307_A, HGDP00127, HGDP00884, HGDP00646, HGDP00654, HGDP00888, HGDP00136, HGDP00428, HGDP00021, 1782681313_A, 1798860592_A, HGDP00787, HGDP00785, HGDP01296, 1780862360_A, HGDP00208, HGDP01352, 1782681296_A, HGDP00143, HGDP00658, HGDP00134, HGDP00364, 1798860569_A, HGDP00681, HGDP01177, 1780854296_A, 1787431196_A
Known GenesANTXRL, ANTXRLP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1109n54
Frequency
Sample Size17421
Observed Gain58
Observed Loss0
Observed Complex0
Frequencyn/a


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