A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115977



Internal ID21299243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:108466968..108472340hg38UCSC Ensembl
Innerchr12:108860745..108866117hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg385373
hg195373
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14091656
Samplessample92
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115977
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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