A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5874n100



Internal ID22791961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:237215..365708hg38UCSC Ensembl
chr6:237215..365708hg19UCSC Ensembl
chr6:182215..310708hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38128494
hg19128494
hg18128494
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1026935, nsv1026239, nsv1022461, nsv1020151, nsv1025992, nsv1029797, nsv1032546, nsv1033008, nsv1030098, nsv1030877, nsv1021209, nsv1020571, nsv1031186, nsv1027063, nsv1030536, nsv1019316, nsv1019802, nsv1031208, nsv1018642, nsv1017293, nsv1026076, nsv1019063, nsv1016599, nsv1020124, nsv1032552, nsv1023739, nsv1024642, nsv1025980, nsv1016766
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)dgv5874n100
Frequency
Sample Size11257
Observed Gain47
Observed Loss0
Observed Complex0
Frequencyn/a


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