A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602326



Internal ID16389735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32498382..32603062hg38UCSC Ensembl
Innerchr6:32466159..32570839hg19UCSC Ensembl
Innerchr6:32574137..32678817hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38104681
hg19104681
hg18104681
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10506n54
Supporting Variantsnssv1055136
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)nsv602326
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