A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545417



Internal ID15986140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:11650504..11661559hg38UCSC Ensembl
Innerchr1:11710561..11721616hg19UCSC Ensembl
Innerchr1:11633148..11644203hg18UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3811056
hg1911056
hg1811056
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv709936
Samples
Known GenesFBXO2, FBXO44
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545417
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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