A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602296



Internal ID16389705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32491473..32534102hg38UCSC Ensembl
Innerchr6:32459250..32501879hg19UCSC Ensembl
Innerchr6:32567228..32609857hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3842630
hg1942630
hg1842630
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10501n54
Supporting Variantsnssv1054964
Samples
Known GenesHLA-DRB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602296
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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