A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5866n100



Internal ID22791953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149649..232061hg38UCSC Ensembl
chr6:149649..232061hg19UCSC Ensembl
chr6:94649..177061hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3882413
hg1982413
hg1882413
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1028502, nsv1030207, nsv1016858
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)dgv5866n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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