A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv371n54



Internal ID18992547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:93823114..93824784hg38UCSC Ensembl
chr1:94288670..94290340hg19UCSC Ensembl
chr1:94061258..94062928hg18UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg381671
hg191671
hg181671
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv546835, nsv546834, nsv546839
Samples
Known GenesBCAR3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv371n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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