A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602555



Internal ID16389964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32556447..32656837hg38UCSC Ensembl
Innerchr6:32524224..32624614hg19UCSC Ensembl
Innerchr6:32632202..32732592hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38100391
hg19100391
hg18100391
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10542n54
Supporting Variantsnssv1055882
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)nsv602555
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