A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562233



Internal ID16349642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:70161932..70198583hg38UCSC Ensembl
Innerchr13:70736064..70772715hg19UCSC Ensembl
Innerchr13:69634065..69670716hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3836652
hg1936652
hg1836652
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3237n54
Supporting Variantsnssv813753, nssv813751, nssv813750, nssv813754, nssv813755, nssv813752, nssv813756
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562233
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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