A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571355



Internal ID16012078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6730568..6811056hg38UCSC Ensembl
Innerchr16:6780569..6861057hg19UCSC Ensembl
Innerchr16:6720570..6801058hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3880489
hg1980489
hg1880489
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv852385
Samples
Known GenesRBFOX1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571355
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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