A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1117n54



Internal ID18993293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46226691..46297471hg38UCSC Ensembl
chr10:47597927..47668707hg19UCSC Ensembl
chr10:47067933..47138713hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3870781
hg1970781
hg1870781
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv550792, nsv550786
SamplesHGDP00574, HGDP01195
Known GenesANTXRL, ANTXRLP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1117n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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