A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602389



Internal ID16389798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32510377..32578039hg38UCSC Ensembl
Innerchr6:32478154..32545816hg19UCSC Ensembl
Innerchr6:32586132..32653794hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3867663
hg1967663
hg1867663
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10523n54
Supporting Variantsnssv1055367, nssv1055366, nssv1055365
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)nsv602389
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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