A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10345n54



Internal ID20143769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29883666..29910961hg38UCSC Ensembl
chr6:29851443..29878738hg19UCSC Ensembl
chr6:29959422..29986717hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3827296
hg1927296
hg1827296
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv601246, nsv601266, nsv601267, nsv601247, nsv601248, nsv601249, nsv601245
Samples
Known GenesHLA-H
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10345n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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