A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7891n54



Internal ID19000067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:44523160..44524882hg38UCSC Ensembl
chr21:45943043..45944765hg19UCSC Ensembl
chr21:44767471..44769193hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg381723
hg191723
hg181723
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv587806, nsv587805
Samples
Known GenesTSPEAR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7891n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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