A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5923n100



Internal ID22792010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:20207662..20260817hg38UCSC Ensembl
chr6:20207893..20261048hg19UCSC Ensembl
chr6:20315872..20369027hg18UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3853156
hg1953156
hg1853156
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1027220, nsv1028657, nsv1027355
Samples
Known GenesMBOAT1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5923n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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