A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv461n21



Internal ID22766653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:78096373..78134460hg38UCSC Ensembl
chr8:79008608..79046695hg19UCSC Ensembl
chr8:79171163..79209250hg18UCSC Ensembl
chr8:79171163..79209250hg17UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg3838088
hg1938088
hg1838088
hg1738088
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv526123, nsv525612
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv461n21
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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