A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602322



Internal ID16389731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32498382..32568117hg38UCSC Ensembl
Innerchr6:32466159..32535894hg19UCSC Ensembl
Innerchr6:32574137..32643872hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3869736
hg1969736
hg1869736
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10514n54
Supporting Variantsnssv1055130, nssv1055131
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)nsv602322
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer