A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571387



Internal ID16012110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6994787..7019055hg38UCSC Ensembl
Innerchr16:7044788..7069056hg19UCSC Ensembl
Innerchr16:6984789..7009057hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3824269
hg1924269
hg1824269
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4899n54
Supporting Variantsnssv852415
Samples
Known GenesRBFOX1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571387
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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