A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602148



Internal ID16389557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32477873..32587882hg38UCSC Ensembl
Innerchr6:32445650..32555659hg19UCSC Ensembl
Innerchr6:32553628..32663637hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38110010
hg19110010
hg18110010
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10492n54
Supporting Variantsnssv1053958
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)nsv602148
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