A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv690n100



Internal ID22786777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:24083364..24102180hg38UCSC Ensembl
chr10:24372293..24391109hg19UCSC Ensembl
chr10:24412299..24431115hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3818817
hg1918817
hg1818817
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1040660, nsv1042219, nsv1040333, nsv1049800
Samples
Known GenesKIAA1217
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv690n100
Frequency
Sample Size11257
Observed Gain12
Observed Loss0
Observed Complex0
Frequencyn/a


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