A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605260



Internal ID16392669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:166570606..167041651hg38UCSC Ensembl
Innerchr6:166984094..167455139hg19UCSC Ensembl
Innerchr6:166904084..167375129hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38471046
hg19471046
hg18471046
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1076263
Samples
Known GenesFGFR1OP, MIR3939, RNASET2, RPS6KA2, RPS6KA2-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605260
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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