A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545642



Internal ID16333051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16259323..16346064hg38UCSC Ensembl
Innerchr1:16585818..16672559hg19UCSC Ensembl
Innerchr1:16458405..16545146hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3886742
hg1986742
hg1886742
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1173786
SamplesHGDP00286
Known GenesFBXO42
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545642
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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