A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590120



Internal ID16377529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:41318043..41744517hg38UCSC Ensembl
Innerchr3:41359534..41786009hg19UCSC Ensembl
Innerchr3:41334538..41761013hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38426475
hg19426476
hg18426476
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8290n54
Supporting Variantsnssv1152249
Samples1798860049_A
Known GenesULK4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590120
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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