A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603447



Internal ID16390856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:65611298..65636196hg38UCSC Ensembl
Innerchr6:66321191..66346089hg19UCSC Ensembl
Innerchr6:66377912..66402810hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3824899
hg1924899
hg1824899
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1062639
Samples
Known GenesEYS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603447
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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