A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546298



Internal ID15987021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:54629436..54641260hg38UCSC Ensembl
Innerchr1:55095109..55106933hg19UCSC Ensembl
Innerchr1:54867697..54879521hg18UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg3811825
hg1911825
hg1811825
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv713478
Samples
Known GenesACOT11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546298
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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