A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1076477



Internal ID15929663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:166748589..166752298hg38UCSC Ensembl
Innerchr6:167162077..167165786hg19UCSC Ensembl
Innerchr6:167082067..167085776hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg383710
hg193710
hg183710
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605279
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)nssv1076477
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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