A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602303



Internal ID16389712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32491715..32627111hg38UCSC Ensembl
Innerchr6:32459492..32594888hg19UCSC Ensembl
Innerchr6:32567470..32702866hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38135397
hg19135397
hg18135397
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10497n54
Supporting Variantsnssv1054977
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)nsv602303
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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