A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153710



Internal ID15873226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:65436926..65522799hg38UCSC Ensembl
Innerchr6:66146819..66232692hg19UCSC Ensembl
Innerchr6:66203540..66289413hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3885874
hg1985874
hg1885874
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv603441
Supporting Variants
SamplesHGDP00146
Known GenesEYS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153710
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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