A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14098987



Internal ID21288028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:41601431..41603600hg38UCSC Ensembl
Innerchr19:42107786..42109955hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg382170
hg192170
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117869
Supporting Variants
Samplessample410
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14098987
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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