A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14100327



Internal ID21269874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40855307..40873143hg38UCSC Ensembl
Innerchr19:41361212..41379048hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3817837
hg1917837
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115574
Supporting Variants
Samplessample144
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14100327
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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