A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602161



Internal ID16389570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32487705..32528971hg38UCSC Ensembl
Innerchr6:32455482..32496748hg19UCSC Ensembl
Innerchr6:32563460..32604726hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3841267
hg1941267
hg1841267
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10501n54
Supporting Variantsnssv1054424, nssv1054426, nssv1054427, nssv1054425
Samples
Known GenesHLA-DRB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602161
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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