A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7107n100



Internal ID20158723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:15545539..15576162hg38UCSC Ensembl
chr8:15403048..15433671hg19UCSC Ensembl
chr8:15447419..15478042hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3830624
hg1930624
hg1830624
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1021634, nsv1030257
Samples
Known GenesTUSC3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7107n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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