A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5893n100



Internal ID22791980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:302294..365708hg38UCSC Ensembl
chr6:302294..365708hg19UCSC Ensembl
chr6:247294..310708hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3863415
hg1963415
hg1863415
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1031319, nsv1018334, nsv1016822, nsv1015877, nsv1015406
Samples
Known GenesDUSP22
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5893n100
Frequency
Sample Size11257
Observed Gain13
Observed Loss0
Observed Complex0
Frequencyn/a


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