A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572829



Internal ID16360238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:58944346..59005195hg38UCSC Ensembl
Innerchr16:58978250..59039099hg19UCSC Ensembl
Innerchr16:57535751..57596600hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3860850
hg1960850
hg1860850
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5167n54
Supporting Variantsnssv858903
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572829
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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