A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10547n54



Internal ID22778442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32551331..32553420hg38UCSC Ensembl
chr6:32519108..32521197hg19UCSC Ensembl
chr6:32627086..32629175hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg382090
hg192090
hg182090
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv602501, nsv602497, nsv602496
Samples
Known GenesHLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10547n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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