A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571375



Internal ID16012098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6848382..6883259hg38UCSC Ensembl
Innerchr16:6898383..6933260hg19UCSC Ensembl
Innerchr16:6838384..6873261hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3834878
hg1934878
hg1834878
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv852403
Samples
Known GenesRBFOX1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571375
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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