A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571583



Internal ID16012306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:19558289..19595586hg38UCSC Ensembl
Innerchr16:19569611..19606908hg19UCSC Ensembl
Innerchr16:19477112..19514409hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3837298
hg1937298
hg1837298
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv852873
Samples
Known GenesC16orf62
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571583
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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