A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5878n100



Internal ID22791965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:252145..385772hg38UCSC Ensembl
chr6:252145..385772hg19UCSC Ensembl
chr6:197145..330772hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38133628
hg19133628
hg18133628
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1027573, nsv1019309, nsv1025932, nsv1035017, nsv1019244, nsv1015612, nsv1035023, nsv1028134, nsv1017828, nsv1027115, nsv1031714, nsv1032943, nsv1021749, nsv1015440, nsv1018450, nsv1016153, nsv1016183, nsv1019993, nsv1029373, nsv1030445, nsv1027524, nsv1030765, nsv1016082, nsv1019881, nsv1017047, nsv1028191, nsv1022899, nsv1022368, nsv1016863, nsv1025122, nsv1035118, nsv1034551, nsv1020521, nsv1025343, nsv1019889, nsv1029144, nsv1024108, nsv1020152, nsv1029211, nsv1021268
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)dgv5878n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss84
Observed Complex0
Frequencyn/a


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