A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112622



Internal ID21295888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:85448903..85504929hg38UCSC Ensembl
Innerchr16:85482509..85538535hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3856027
hg1956027
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14098210
Samplessample5
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112622
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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