A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591889



Internal ID16032612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:141051054..141059296hg38UCSC Ensembl
Innerchr3:140769896..140778138hg19UCSC Ensembl
Innerchr3:142252586..142260828hg18UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg388243
hg198243
hg188243
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv975053
Samples
Known GenesSPSB4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591889
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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