A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7879n54



Internal ID22775774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:44199484..44208491hg38UCSC Ensembl
chr21:45619367..45628374hg19UCSC Ensembl
chr21:44443795..44452802hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg389008
hg199008
hg189008
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv587738, nsv587730
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7879n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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