A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546186



Internal ID16333595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:47416969..47417352hg38UCSC Ensembl
Innerchr1:47882641..47883024hg19UCSC Ensembl
Innerchr1:47655228..47655611hg18UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg38384
hg19384
hg18384
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv264n54
Supporting Variantsnssv712954, nssv712955
Samples
Known GenesFOXE3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546186
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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