A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1055888



Internal ID15909074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32556447..32658394hg38UCSC Ensembl
Innerchr6:32524224..32626171hg19UCSC Ensembl
Innerchr6:32632202..32734149hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38101948
hg19101948
hg18101948
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602558
Supporting Variants
Samples
Known GenesHLA-DQA1, HLA-DRB1, HLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1055888
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer