A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602272



Internal ID16389681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32491135..32592854hg38UCSC Ensembl
Innerchr6:32458912..32560631hg19UCSC Ensembl
Innerchr6:32566890..32668609hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38101720
hg19101720
hg18101720
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10506n54
Supporting Variantsnssv1054905
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)nsv602272
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