A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571327



Internal ID16012050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6509061..6615623hg38UCSC Ensembl
Innerchr16:6559062..6665624hg19UCSC Ensembl
Innerchr16:6499063..6605625hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38106563
hg19106563
hg18106563
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv852363
Samples
Known GenesRBFOX1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571327
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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