A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589954



Internal ID16377363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:24925277..25030125hg38UCSC Ensembl
Innerchr3:24966768..25071616hg19UCSC Ensembl
Innerchr3:24941772..25046620hg18UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg38104849
hg19104849
hg18104849
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151764
SamplesHGDP00884
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589954
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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