A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603437



Internal ID16390846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:65342401..65412466hg38UCSC Ensembl
Innerchr6:66052294..66122359hg19UCSC Ensembl
Innerchr6:66109015..66179080hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3870066
hg1970066
hg1870066
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10726n54
Supporting Variantsnssv1062634
Samples
Known GenesEYS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603437
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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