A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546162



Internal ID15986885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:46341925..46405089hg38UCSC Ensembl
Innerchr1:46807597..46870761hg19UCSC Ensembl
Innerchr1:46580184..46643348hg18UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg3863165
hg1963165
hg1863165
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv712899
Samples
Known GenesFAAH, NSUN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546162
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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