A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7877n54



Internal ID19000053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:43740172..43740914hg38UCSC Ensembl
chr21:45160053..45160795hg19UCSC Ensembl
chr21:43984481..43985223hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38743
hg19743
hg18743
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv587713, nsv587715
Samples
Known GenesPDXK
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7877n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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