A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602175



Internal ID16389584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32487705..32563468hg38UCSC Ensembl
Innerchr6:32455482..32531245hg19UCSC Ensembl
Innerchr6:32563460..32639223hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3875764
hg1975764
hg1875764
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10503n54
Supporting Variantsnssv1054468, nssv1054471, nssv1054473, nssv1054470, nssv1054469, nssv1054472
Samples
Known GenesHLA-DRB5, HLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602175
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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