A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571379



Internal ID16012102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6869983..7019055hg38UCSC Ensembl
Innerchr16:6919984..7069056hg19UCSC Ensembl
Innerchr16:6859985..7009057hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38149073
hg19149073
hg18149073
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4897n54
Supporting Variantsnssv852407
Samples
Known GenesRBFOX1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571379
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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