A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7266n100



Internal ID22793353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:88824545..88939682hg38UCSC Ensembl
chr8:89836774..89951911hg19UCSC Ensembl
chr8:89905890..90021027hg18UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38115138
hg19115138
hg18115138
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1029213, nsv1018348
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7266n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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