A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605333



Internal ID16392742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:166787545..166908205hg38UCSC Ensembl
Innerchr6:167201033..167321693hg19UCSC Ensembl
Innerchr6:167121023..167241683hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38120661
hg19120661
hg18120661
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1076678
Samples
Known GenesRPS6KA2, RPS6KA2-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605333
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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