A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv928n100



Internal ID19011296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:75223392..75325170hg38UCSC Ensembl
chr10:76983150..77084928hg19UCSC Ensembl
chr10:76653156..76754934hg18UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38101779
hg19101779
hg18101779
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1053530, nsv1035825, nsv1050461
Samples
Known GenesCOMTD1, VDAC2, ZNF503-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv928n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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