A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605327



Internal ID16046050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:166772186..166946901hg38UCSC Ensembl
Innerchr6:167185674..167360389hg19UCSC Ensembl
Innerchr6:167105664..167280379hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38174716
hg19174716
hg18174716
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11053n54
Supporting Variantsnssv1076636
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)nsv605327
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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