A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14094576



Internal ID21281461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:236659804..236671065hg38UCSC Ensembl
Innerchr1:236823104..236834365hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg3811262
hg1911262
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110739
Supporting Variants
Samplessample312
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14094576
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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