A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv666n100



Internal ID20152282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5920672..6010233hg38UCSC Ensembl
chr10:5962635..6052196hg19UCSC Ensembl
chr10:6002641..6092202hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3889562
hg1989562
hg1889562
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1041261, nsv1050983
Samples
Known GenesFBXO18, IL15RA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv666n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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