A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101236



Internal ID21292268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:39538921..39540804hg38UCSC Ensembl
Innerchr19:40029561..40031444hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg381884
hg191884
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117096
Supporting Variants
Samplessample86
Known GenesEID2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101236
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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