A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10884n54



Internal ID22778779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:103340397..103395694hg38UCSC Ensembl
chr6:103788272..103843569hg19UCSC Ensembl
chr6:103894965..103950262hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3855298
hg1955298
hg1855298
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv604382, nsv604383
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10884n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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