A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571266



Internal ID16358675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:3880210..3881031hg38UCSC Ensembl
Innerchr16:3930211..3931032hg19UCSC Ensembl
Innerchr16:3870212..3871033hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38822
hg19822
hg18822
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv852283, nssv852282
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571266
Frequency
Sample Size17421
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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