A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7926n54



Internal ID22775821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:46237682..46238490hg38UCSC Ensembl
chr21:47657596..47658404hg19UCSC Ensembl
chr21:46482024..46482832hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38809
hg19809
hg18809
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv587969, nsv587971
Samples
Known GenesMCM3AP, MCM3AP-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7926n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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