A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14090425



Internal ID21267439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:236378701..236391902hg38UCSC Ensembl
Innerchr1:236542001..236555202hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg3813202
hg1913202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115075
Supporting Variants
Samplessample112
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14090425
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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