A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602406



Internal ID16389815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32519533..32522155hg38UCSC Ensembl
Innerchr6:32487310..32489932hg19UCSC Ensembl
Innerchr6:32595288..32597910hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg382623
hg192623
hg182623
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1055411, nssv1055413, nssv1055415, nssv1055412, nssv1055414, nssv1055416
Samples
Known GenesHLA-DRB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602406
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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