A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv249n21



Internal ID22766441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:56440110..56445633hg38UCSC Ensembl
chr20:55015166..55020689hg19UCSC Ensembl
chr20:54448573..54454096hg18UCSC Ensembl
chr20:54448573..54454096hg17UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg385524
hg195524
hg185524
hg175524
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv524572, nsv519169
Samples
Known GenesCASS4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv249n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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