A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5882n100



Internal ID22791969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:254255..322696hg38UCSC Ensembl
chr6:254255..322696hg19UCSC Ensembl
chr6:199255..267696hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3868442
hg1968442
hg1868442
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1018616, nsv1024900, nsv1024491, nsv1032709, nsv1034170, nsv1030954, nsv1027480, nsv1026960, nsv1033255, nsv1019410
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)dgv5882n100
Frequency
Sample Size11257
Observed Gain31
Observed Loss34
Observed Complex0
Frequencyn/a


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