A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1107n54



Internal ID20134531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46166132..46269108hg38UCSC Ensembl
chr10:47537368..47640344hg19UCSC Ensembl
chr10:47007374..47110350hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38102977
hg19102977
hg18102977
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv550740, nsv550730, nsv550741, nsv550739, nsv550738
SamplesHGDP01413, HGDP00907, HGDP00925
Known GenesANTXRLP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1107n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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