A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602158



Internal ID16389567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32487705..32517715hg38UCSC Ensembl
Innerchr6:32455482..32485492hg19UCSC Ensembl
Innerchr6:32563460..32593470hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3830011
hg1930011
hg1830011
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10498n54
Supporting Variantsnssv1054347, nssv1054349, nssv1054348
Samples
Known GenesHLA-DRB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602158
Frequency
Sample Size17421
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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