A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5891n100



Internal ID22791978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:290586..366333hg38UCSC Ensembl
chr6:290586..366333hg19UCSC Ensembl
chr6:235586..311333hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3875748
hg1975748
hg1875748
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1034818, nsv1032728
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)dgv5891n100
Frequency
Sample Size11257
Observed Gain13
Observed Loss2
Observed Complex0
Frequencyn/a


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