A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv902n100



Internal ID22786989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:66489541..66776296hg38UCSC Ensembl
chr10:68249299..68536054hg19UCSC Ensembl
chr10:67919305..68206060hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38286756
hg19286756
hg18286756
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1049411, nsv1048376, nsv1037600
Samples
Known GenesCTNNA3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv902n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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