A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589440



Internal ID16030163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4106646..4245016hg38UCSC Ensembl
Innerchr3:4148330..4286700hg19UCSC Ensembl
Innerchr3:4123330..4261700hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38138371
hg19138371
hg18138371
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8183n54
Supporting Variantsnssv958035
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589440
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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