A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602719



Internal ID16390128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32641154..32643220hg38UCSC Ensembl
Innerchr6:32608931..32610997hg19UCSC Ensembl
Innerchr6:32716909..32718975hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg382067
hg192067
hg182067
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10589n54
Supporting Variantsnssv1056539
Samples
Known GenesHLA-DQA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602719
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