A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10487n54



Internal ID22778382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32462952..32538126hg38UCSC Ensembl
chr6:32430729..32505903hg19UCSC Ensembl
chr6:32538707..32613881hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3875175
hg1975175
hg1875175
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv602113, nsv602126
Samples
Known GenesHLA-DRB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10487n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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