A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589446



Internal ID16030169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4153765..4236779hg38UCSC Ensembl
Innerchr3:4195449..4278463hg19UCSC Ensembl
Innerchr3:4170449..4253463hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3883015
hg1983015
hg1883015
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8184n54
Supporting Variantsnssv958045
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589446
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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