A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571360



Internal ID16012083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6753844..6774822hg38UCSC Ensembl
Innerchr16:6803845..6824823hg19UCSC Ensembl
Innerchr16:6743846..6764824hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3820979
hg1920979
hg1820979
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv852390
Samples
Known GenesRBFOX1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571360
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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