A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10488n54



Internal ID22778383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32462952..32592550hg38UCSC Ensembl
chr6:32430729..32560327hg19UCSC Ensembl
chr6:32538707..32668305hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38129599
hg19129599
hg18129599
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv602127, nsv602115, nsv602116, nsv602125, nsv602120, nsv602121, nsv602114, nsv602124
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)dgv10488n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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