A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv19n54



Internal ID20133443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:1028484..1045080hg38UCSC Ensembl
chr1:963864..980460hg19UCSC Ensembl
chr1:953727..970323hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3816597
hg1916597
hg1816597
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv544940, nsv544944
Samples
Known GenesAGRN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv19n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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