A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7892n54



Internal ID19000068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:44523514..44525236hg38UCSC Ensembl
chr21:45943397..45945119hg19UCSC Ensembl
chr21:44767825..44769547hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg381723
hg191723
hg181723
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv587807, nsv587809, nsv587808
Samples
Known GenesTSPEAR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7892n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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