A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591890



Internal ID16379299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:141058149..141059296hg38UCSC Ensembl
Innerchr3:140776991..140778138hg19UCSC Ensembl
Innerchr3:142259681..142260828hg18UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg381148
hg191148
hg181148
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv975054, nssv975058, nssv975055, nssv975057, nssv975056
Samples
Known GenesSPSB4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591890
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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