A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602519



Internal ID16389928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32554310..32556447hg38UCSC Ensembl
Innerchr6:32522087..32524224hg19UCSC Ensembl
Innerchr6:32630065..32632202hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg382138
hg192138
hg182138
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10555n54
Supporting Variantsnssv1055756, nssv1055753, nssv1055750, nssv1055744, nssv1055738, nssv1055742, nssv1055740, nssv1055745, nssv1055755, nssv1055754, nssv1055749, nssv1055751, nssv1055748, nssv1055752, nssv1055741, nssv1055739, nssv1055743, nssv1055747, nssv1055746
Samples
Known GenesHLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602519
Frequency
Sample Size17421
Observed Gain0
Observed Loss19
Observed Complex0
Frequencyn/a


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