A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602308



Internal ID16389717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32492173..32591169hg38UCSC Ensembl
Innerchr6:32459950..32558946hg19UCSC Ensembl
Innerchr6:32567928..32666924hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3898997
hg1998997
hg1898997
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10506n54
Supporting Variantsnssv1054982
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)nsv602308
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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