A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602413



Internal ID16389822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32521954..32530183hg38UCSC Ensembl
Innerchr6:32489731..32497960hg19UCSC Ensembl
Innerchr6:32597709..32605938hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg388230
hg198230
hg188230
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10528n54
Supporting Variantsnssv1055513, nssv1055512, nssv1055510, nssv1055515, nssv1055511, nssv1055514
Samples
Known GenesHLA-DRB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602413
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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