A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv110n97



Internal ID22815507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:21368130..21594646hg38UCSC Ensembl
chr16:21379451..21605967hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38226517
hg19226517
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1155274, nsv1155277, nsv1155279, nsv1155271, nsv1155272, nsv1155276, nsv1155275, nsv1155278
Samples
Known GenesLOC100190986, LOC100271836, NPIPB3, SLC7A5P2, SNX29P1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv110n97
Frequency
Sample Size131
Observed Gain121
Observed Loss0
Observed Complex0
Frequencyn/a


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