A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv893n100



Internal ID22786980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:66158287..66330108hg38UCSC Ensembl
chr10:67918045..68089866hg19UCSC Ensembl
chr10:67588051..67759872hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38171822
hg19171822
hg18171822
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1054749, nsv1035405, nsv1041921
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)dgv893n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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