A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1055564



Internal ID15908750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32526201..32577369hg38UCSC Ensembl
Innerchr6:32493978..32545146hg19UCSC Ensembl
Innerchr6:32601956..32653124hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3851169
hg1951169
hg1851169
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602423
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)nssv1055564
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