A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602120



Internal ID16389529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32463515..32582158hg38UCSC Ensembl
Innerchr6:32431292..32549935hg19UCSC Ensembl
Innerchr6:32539270..32657913hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38118644
hg19118644
hg18118644
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10488n54
Supporting Variantsnssv1053922
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)nsv602120
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