A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5952n100



Internal ID22792039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:33827894..33879568hg38UCSC Ensembl
chr6:33795671..33847345hg19UCSC Ensembl
chr6:33903649..33955323hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3851675
hg1951675
hg1851675
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1022403, nsv1032074
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5952n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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