A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573719



Internal ID16014442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88933306..88957164hg38UCSC Ensembl
Innerchr16:88999714..89023572hg19UCSC Ensembl
Innerchr16:87527215..87551073hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3823859
hg1923859
hg1823859
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv863303, nssv863304
Samples
Known GenesCBFA2T3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573719
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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