A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv280n54



Internal ID20133704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:54627627..54628371hg38UCSC Ensembl
chr1:55093300..55094044hg19UCSC Ensembl
chr1:54865888..54866632hg18UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38745
hg19745
hg18745
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv546282, nsv546280, nsv546281, nsv546279, nsv546285, nsv546289
Samples
Known GenesACOT11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv280n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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