A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602332



Internal ID16389741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32501123..32519392hg38UCSC Ensembl
Innerchr6:32468900..32487169hg19UCSC Ensembl
Innerchr6:32576878..32595147hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3818270
hg1918270
hg1818270
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10517n54
Supporting Variantsnssv1055150
Samples
Known GenesHLA-DRB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602332
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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