A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602354



Internal ID16389763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32504616..32521324hg38UCSC Ensembl
Innerchr6:32472393..32489101hg19UCSC Ensembl
Innerchr6:32580371..32597079hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3816709
hg1916709
hg1816709
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10517n54
Supporting Variantsnssv1055224
Samples
Known GenesHLA-DRB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602354
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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