A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7295n100



Internal ID22793382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:114615055..114638558hg38UCSC Ensembl
chr8:115627284..115650787hg19UCSC Ensembl
chr8:115696460..115719963hg18UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3823504
hg1923504
hg1823504
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1025424, nsv1018696
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)dgv7295n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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