A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571391



Internal ID16012114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:7056359..7076731hg38UCSC Ensembl
Innerchr16:7106360..7126732hg19UCSC Ensembl
Innerchr16:7046361..7066733hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3820373
hg1920373
hg1820373
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150509
SamplesHGDP00808
Known GenesRBFOX1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571391
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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