A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4278n100



Internal ID22790365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:15321244..15337332hg38UCSC Ensembl
chr20:15301890..15317978hg19UCSC Ensembl
chr20:15249890..15265978hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3816089
hg1916089
hg1816089
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1057619, nsv1055943
Samples
Known GenesMACROD2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4278n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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