A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10557n54



Internal ID22778452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32555036..32565053hg38UCSC Ensembl
chr6:32522813..32532830hg19UCSC Ensembl
chr6:32630791..32640808hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3810018
hg1910018
hg1810018
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv602538, nsv602540, nsv602548, nsv602539
Samples
Known GenesHLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10557n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss22
Observed Complex0
Frequencyn/a


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