A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv662n100



Internal ID20152278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4229680..4264606hg38UCSC Ensembl
chr10:4271872..4306798hg19UCSC Ensembl
chr10:4261872..4296798hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3834927
hg1934927
hg1834927
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1044535, nsv1053322
Samples
Known GenesLINC00702
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv662n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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