A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv586n54



Internal ID20134010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:157203964..157205449hg38UCSC Ensembl
chr1:157173754..157175239hg19UCSC Ensembl
chr1:155440378..155441863hg18UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg381486
hg191486
hg181486
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv547975, nsv547970, nsv547971, nsv547976, nsv547972, nsv547969, nsv547973
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv586n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss82
Observed Complex0
Frequencyn/a


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