A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14100336



Internal ID21270025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:13765734..13768825hg38UCSC Ensembl
Innerchr19:13876548..13879639hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg383092
hg193092
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115252
Supporting Variants
Samplessample146
Known GenesMRI1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14100336
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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