A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603392



Internal ID16044115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:64433115..65604257hg38UCSC Ensembl
Innerchr6:65143008..66314150hg19UCSC Ensembl
Innerchr6:65199729..66370871hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg381171143
hg191171143
hg181171143
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1061737
Samples
Known GenesEYS, LOC441155
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603392
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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