A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571341



Internal ID16012064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6611646..6622410hg38UCSC Ensembl
Innerchr16:6661647..6672411hg19UCSC Ensembl
Innerchr16:6601648..6612412hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3810765
hg1910765
hg1810765
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv852372
Samples
Known GenesRBFOX1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571341
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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