A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571731



Internal ID16359140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:28403071..28415283hg38UCSC Ensembl
Innerchr16:28414392..28426604hg19UCSC Ensembl
Innerchr16:28321893..28334105hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3812213
hg1912213
hg1812213
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4967n54
Supporting Variantsnssv855259
Samples
Known GenesEIF3C, EIF3CL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571731
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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