A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602411



Internal ID16389820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32521382..32530091hg38UCSC Ensembl
Innerchr6:32489159..32497868hg19UCSC Ensembl
Innerchr6:32597137..32605846hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg388710
hg198710
hg188710
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10528n54
Supporting Variantsnssv1055424
Samples
Known GenesHLA-DRB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602411
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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