A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv965n100



Internal ID19011333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103385173..103457152hg38UCSC Ensembl
chr10:105144930..105216909hg19UCSC Ensembl
chr10:105134920..105206899hg18UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg3871980
hg1971980
hg1871980
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1053123, nsv1036069
Samples
Known GenesCALHM1, CALHM2, MIR1307, PDCD11, TAF5, USMG5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv965n100
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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