A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1076677



Internal ID15929863
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 StatusS
Merged Variantsnsv605332
Supporting Variants
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)nssv1076677
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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