A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7932n54



Internal ID22775827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:46382747..46384034hg38UCSC Ensembl
chr21:47802662..47803949hg19UCSC Ensembl
chr21:46627090..46628377hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg381288
hg191288
hg181288
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv587989, nsv587985, nsv587990
Samples
Known GenesPCNT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7932n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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