A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605332



Internal ID16392741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:166784539..166940213hg38UCSC Ensembl
Innerchr6:167198027..167353701hg19UCSC Ensembl
Innerchr6:167118017..167273691hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38155675
hg19155675
hg18155675
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11053n54
Supporting Variantsnssv1076677
Samples
Known GenesRNASET2, RPS6KA2, RPS6KA2-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605332
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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