A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590482



Internal ID16377891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:65199224..65226921hg38UCSC Ensembl
Innerchr3:65184899..65212596hg19UCSC Ensembl
Innerchr3:65159939..65187636hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3827698
hg1927698
hg1827698
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8353n54
Supporting Variantsnssv963704, nssv963703, nssv963694, nssv963698, nssv963691, nssv1151917, nssv963699, nssv963688, nssv963697, nssv963695, nssv963696, nssv963690, nssv963693, nssv963687, nssv963702, nssv963692, nssv963686, nssv963700, nssv963701, nssv1151915, nssv1151914, nssv963689, nssv1151916, nssv963685, nssv1151913
Samples1782681144_A, 1780862388_A, 1780854096_A, 1780854340_A, 1780854063_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590482
Frequency
Sample Size17421
Observed Gain0
Observed Loss25
Observed Complex0
Frequencyn/a


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