A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589852



Internal ID16030575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:18318496..18345841hg38UCSC Ensembl
Innerchr3:18359988..18387333hg19UCSC Ensembl
Innerchr3:18334992..18362337hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3827346
hg1927346
hg1827346
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv959874
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589852
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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