A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562238



Internal ID16349647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:70165521..70198524hg38UCSC Ensembl
Innerchr13:70739653..70772656hg19UCSC Ensembl
Innerchr13:69637654..69670657hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3833004
hg1933004
hg1833004
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3237n54
Supporting Variantsnssv813775, nssv813776, nssv813785, nssv813786, nssv813771, nssv813783, nssv813781, nssv813773, nssv813778, nssv813779, nssv813787, nssv813777, nssv813782, nssv813784, nssv813774, nssv813772, nssv813770, nssv813780
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562238
Frequency
Sample Size17421
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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