A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14099494



Internal ID21291699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:25034095..25037451hg38UCSC Ensembl
Innerchr18:22614059..22617415hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg383357
hg193357
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114446
Supporting Variants
Samplessample78
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14099494
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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