A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572514



Internal ID16359923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:46418653..46466390hg38UCSC Ensembl
Innerchr16:46452565..46500302hg19UCSC Ensembl
Innerchr16:45010066..45057803hg18UCSC Ensembl
Cytoband16q11.2
Allele length
AssemblyAllele length
hg3847738
hg1947738
hg1847738
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5105n54
Supporting Variantsnssv856615
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572514
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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