A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589958



Internal ID16377367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:25864102..26144282hg38UCSC Ensembl
Innerchr3:25905593..26185773hg19UCSC Ensembl
Innerchr3:25880597..26160777hg18UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg38280181
hg19280181
hg18280181
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv960129
Samples
Known GenesLINC00692
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589958
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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