A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603439



Internal ID16390848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:65405761..65522799hg38UCSC Ensembl
Innerchr6:66115654..66232692hg19UCSC Ensembl
Innerchr6:66172375..66289413hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38117039
hg19117039
hg18117039
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1153709
Samples1780862042_A
Known GenesEYS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603439
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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