A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10344n54



Internal ID20143768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29879365..29933791hg38UCSC Ensembl
chr6:29847142..29901568hg19UCSC Ensembl
chr6:29955121..30009547hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3854427
hg1954427
hg1854427
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv601255, nsv601243, nsv601254, nsv601252, nsv601251, nsv601253, nsv601256, nsv601244, nsv601271
Samples
Known GenesHCG4B, HLA-H
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10344n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss47
Observed Complex0
Frequencyn/a


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