A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7901n54



Internal ID22775796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:45426100..45479205hg38UCSC Ensembl
chr21:46846015..46899119hg19UCSC Ensembl
chr21:45670443..45723547hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3853106
hg1953105
hg1853105
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv587846, nsv587845
Samples
Known GenesCOL18A1, MIR6815
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7901n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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