A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590187



Internal ID16377596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46755146..46789244hg38UCSC Ensembl
Innerchr3:46796636..46830734hg19UCSC Ensembl
Innerchr3:46771640..46805738hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3834099
hg1934099
hg1834099
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8306n54
Supporting Variantsnssv962546, nssv962545, nssv962543, nssv962544
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590187
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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