A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1113n54



Internal ID20134537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46215343..46332710hg38UCSC Ensembl
chr10:47586579..47703946hg19UCSC Ensembl
chr10:47056585..47173952hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38117368
hg19117368
hg18117368
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv550773, nsv550772, nsv550768
Samples
Known GenesANTXRL, ANTXRLP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1113n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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