A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572471



Internal ID16359880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:46402779..46465763hg38UCSC Ensembl
Innerchr16:46436691..46499675hg19UCSC Ensembl
Innerchr16:44994192..45057176hg18UCSC Ensembl
Cytoband16q11.2
Allele length
AssemblyAllele length
hg3862985
hg1962985
hg1862985
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5102n54
Supporting Variantsnssv856550
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572471
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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