A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10497n54



Internal ID22778392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32486077..32627111hg38UCSC Ensembl
chr6:32453854..32594888hg19UCSC Ensembl
chr6:32561832..32702866hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38141035
hg19141035
hg18141035
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv602274, nsv602303, nsv602221, nsv602153
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)dgv10497n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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