A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602258



Internal ID16389667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32491135..32574356hg38UCSC Ensembl
Innerchr6:32458912..32542133hg19UCSC Ensembl
Innerchr6:32566890..32650111hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3883222
hg1983222
hg1883222
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10506n54
Supporting Variantsnssv1054816, nssv1054813, nssv1054810, nssv1054827, nssv1054808, nssv1054821, nssv1054823, nssv1054815, nssv1054811, nssv1054826, nssv1054807, nssv1054829, nssv1054822, nssv1054828, nssv1054825, nssv1054814, nssv1054820, nssv1054831, nssv1054812, nssv1054818, nssv1054832, nssv1054809, nssv1054824, nssv1054819, nssv1054817, nssv1054830
Samples
Known GenesHLA-DRB5, HLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602258
Frequency
Sample Size17421
Observed Gain0
Observed Loss26
Observed Complex0
Frequencyn/a


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