A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602408



Internal ID16389817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32519533..32530183hg38UCSC Ensembl
Innerchr6:32487310..32497960hg19UCSC Ensembl
Innerchr6:32595288..32605938hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3810651
hg1910651
hg1810651
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10528n54
Supporting Variantsnssv1055419
Samples
Known GenesHLA-DRB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602408
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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