A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117552



Internal ID21300818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:89966004..89970879hg38UCSC Ensembl
Innerchr1:90431563..90436438hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg384876
hg194876
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14086620
Samplessample205
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117552
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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