A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7299n100



Internal ID22793386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:115039025..115141777hg38UCSC Ensembl
chr8:116051254..116154006hg19UCSC Ensembl
chr8:116120430..116223182hg18UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg38102753
hg19102753
hg18102753
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1032185, nsv1025482, nsv1029474, nsv1016140, nsv1025666
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)dgv7299n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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