A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1119n54



Internal ID20134543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46306562..46379219hg38UCSC Ensembl
chr10:47677798..47750479hg19UCSC Ensembl
chr10:47147804..47220485hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3872658
hg1972682
hg1872682
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv550799, nsv550798
Samples
Known GenesANTXRL, ANXA8L1, ANXA8L2, FAM25B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1119n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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