A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603396



Internal ID16390805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:64611796..64769301hg38UCSC Ensembl
Innerchr6:65321689..65479194hg19UCSC Ensembl
Innerchr6:65378410..65535915hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38157506
hg19157506
hg18157506
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1061739
Samples
Known GenesEYS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603396
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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