A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1076282



Internal ID15929468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:166748083..166749719hg38UCSC Ensembl
Innerchr6:167161571..167163207hg19UCSC Ensembl
Innerchr6:167081561..167083197hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381637
hg191637
hg181637
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605265
Supporting Variants
Samples
Known GenesRPS6KA2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1076282
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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