A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602263



Internal ID16389672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32491135..32582158hg38UCSC Ensembl
Innerchr6:32458912..32549935hg19UCSC Ensembl
Innerchr6:32566890..32657913hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3891024
hg1991024
hg1891024
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10506n54
Supporting Variantsnssv1054851, nssv1054854, nssv1054855, nssv1054845, nssv1054847, nssv1054853, nssv1054848, nssv1054850, nssv1054852, nssv1054849, nssv1054846
Samples
Known GenesHLA-DRB1, HLA-DRB5, HLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602263
Frequency
Sample Size17421
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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