A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1108n54



Internal ID20134532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46166132..46295928hg38UCSC Ensembl
chr10:47537368..47667164hg19UCSC Ensembl
chr10:47007374..47137170hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38129797
hg19129797
hg18129797
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv550745, nsv550744, nsv550747, nsv550746, nsv550731
SamplesHGDP00621
Known GenesANTXRL, ANTXRLP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1108n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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