A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602365



Internal ID16389774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32505399..32583827hg38UCSC Ensembl
Innerchr6:32473176..32551604hg19UCSC Ensembl
Innerchr6:32581154..32659582hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3878429
hg1978429
hg1878429
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10523n54
Supporting Variantsnssv1055243
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)nsv602365
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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