A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7226n100



Internal ID22793313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:53615706..53679513hg38UCSC Ensembl
chr8:54528266..54592073hg19UCSC Ensembl
chr8:54690819..54754626hg18UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg3863808
hg1963808
hg1863808
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1020081, nsv1030947
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)dgv7226n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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