A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7277n100



Internal ID22793364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:101375798..101390702hg38UCSC Ensembl
chr8:102388026..102402930hg19UCSC Ensembl
chr8:102457202..102472106hg18UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3814905
hg1914905
hg1814905
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1026102, nsv1024783, nsv1024285
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)dgv7277n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss21
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer