A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv107n97



Internal ID22815504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:18153433..18768126hg38UCSC Ensembl
chr16:18247290..18779448hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38614694
hg19532159
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1155262, nsv1155261, nsv1155260, nsv1155258, nsv1155259
Samples
Known GenesABCC6P1, LOC100288162, MIR3179-1, MIR3179-2, MIR3179-3, MIR3180-1, MIR3180-2, MIR3180-3, MIR6511A-2, MIR6770-2, NOMO2, NPIPA7, NPIPA8
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv107n97
Frequency
Sample Size131
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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