A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590983



Internal ID16378392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:90269478..90455495hg38UCSC Ensembl
Innerchr3:90318628..90504645hg19UCSC Ensembl
Innerchr3:90401318..90587335hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg38186018
hg19186018
hg18186018
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8442n54
Supporting Variantsnssv967768
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590983
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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