A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3057n100



Internal ID20154673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:84378422..84500091hg38UCSC Ensembl
chr16:84412028..84533697hg19UCSC Ensembl
chr16:82969529..83091198hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38121670
hg19121670
hg18121670
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1067042, nsv1064903
Samples
Known GenesATP2C2, TLDC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3057n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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