A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv916n100



Internal ID20152532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:66975498..67173658hg38UCSC Ensembl
chr10:68735256..68933416hg19UCSC Ensembl
chr10:68405262..68603422hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38198161
hg19198161
hg18198161
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1036534, nsv1037907, nsv1044293, nsv1037547
Samples
Known GenesCTNNA3, LRRTM3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv916n100
Frequency
Sample Size29084
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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