A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1054456



Internal ID15907642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32487705..32560016hg38UCSC Ensembl
Innerchr6:32455482..32527793hg19UCSC Ensembl
Innerchr6:32563460..32635771hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3872312
hg1972312
hg1872312
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602173
Supporting Variants
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)nssv1054456
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