A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3060n100



Internal ID19013428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85694893..85772099hg38UCSC Ensembl
chr16:85728499..85805705hg19UCSC Ensembl
chr16:84286000..84363206hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3877207
hg1977207
hg1877207
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1058951, nsv1057769
Samples
Known GenesC16orf74, MIR1910, MIR7851
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3060n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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