A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589441



Internal ID16030164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4140066..4242079hg38UCSC Ensembl
Innerchr3:4181750..4283763hg19UCSC Ensembl
Innerchr3:4156750..4258763hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38102014
hg19102014
hg18102014
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8184n54
Supporting Variantsnssv958036, nssv958037
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589441
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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