A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111182



Internal ID21294448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:87302288..87307340hg38UCSC Ensembl
Innerchr16:87335894..87340946hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg385053
hg195053
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14099154
Samplessample157
Known GenesC16orf95
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111182
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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