A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3058n100



Internal ID19013426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:84574421..84612845hg38UCSC Ensembl
chr16:84608027..84646451hg19UCSC Ensembl
chr16:83165528..83203952hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3838425
hg1938425
hg1838425
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1058311, nsv1062836
Samples
Known GenesCOTL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3058n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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