A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590920



Internal ID16378329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:87911096..87920412hg38UCSC Ensembl
Innerchr3:87960246..87969562hg19UCSC Ensembl
Innerchr3:88042936..88052252hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg389317
hg199317
hg189317
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv967560
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590920
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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