A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv455n21



Internal ID22766647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:25688240..25794084hg38UCSC Ensembl
chr8:25545756..25651600hg19UCSC Ensembl
chr8:25601673..25707517hg18UCSC Ensembl
chr8:25601673..25707517hg17UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg38105845
hg19105845
hg18105845
hg17105845
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv522868, nsv520516
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv455n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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