A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603391



Internal ID16044114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:64261543..64488322hg38UCSC Ensembl
Innerchr6:64971436..65198215hg19UCSC Ensembl
Innerchr6:65029395..65254936hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38226780
hg19226780
hg18225542
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1061736
Samples
Known GenesEYS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603391
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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