A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv452n21



Internal ID18990925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:24421431..24505297hg38UCSC Ensembl
chr8:24278944..24362810hg19UCSC Ensembl
chr8:24334889..24418700hg18UCSC Ensembl
chr8:24334889..24418700hg17UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3883867
hg1983867
hg1883812
hg1783812
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv521359, nsv518606
Samples
Known GenesADAM7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv452n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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