A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572393



Internal ID16359802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:35918519..35985178hg38UCSC Ensembl
Innerchr16:35152890..35219549hg19UCSC Ensembl
Innerchr16:35010391..35077050hg18UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg3866660
hg1966660
hg1866660
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5086n54
Supporting Variantsnssv856268
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572393
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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