A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572467



Internal ID16359876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:46401993..46466097hg38UCSC Ensembl
Innerchr16:46435905..46500009hg19UCSC Ensembl
Innerchr16:44993406..45057510hg18UCSC Ensembl
Cytoband16q11.2
Allele length
AssemblyAllele length
hg3864105
hg1964105
hg1864105
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5102n54
Supporting Variantsnssv856531, nssv856532
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572467
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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