A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv379n54



Internal ID20133803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:101808720..101838596hg38UCSC Ensembl
chr1:102274276..102304152hg19UCSC Ensembl
chr1:102046864..102076740hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3829877
hg1929877
hg1829877
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv546899, nsv546898
Samples
Known GenesOLFM3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv379n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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