A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589426



Internal ID16030149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4079225..4188112hg38UCSC Ensembl
Innerchr3:4120909..4229796hg19UCSC Ensembl
Innerchr3:4095909..4204796hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38108888
hg19108888
hg18108888
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8179n54
Supporting Variantsnssv958025, nssv958026
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589426
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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