A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602267



Internal ID16389676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32491135..32587882hg38UCSC Ensembl
Innerchr6:32458912..32555659hg19UCSC Ensembl
Innerchr6:32566890..32663637hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3896748
hg1996748
hg1896748
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10504n54
Supporting Variantsnssv1054861, nssv1054862
Samples
Known GenesHLA-DRB1, HLA-DRB5, HLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602267
Frequency
Sample Size17421
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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