A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10365n54



Internal ID22778260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29942940..29945360hg38UCSC Ensembl
chr6:29910717..29913137hg19UCSC Ensembl
chr6:30018696..30021116hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg382421
hg192421
hg182421
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv601459, nsv601460, nsv601461
Samples
Known GenesHLA-A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10365n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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