A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101499



Internal ID21284536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:6690214..6693221hg38UCSC Ensembl
Innerchr19:6690225..6693232hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg383008
hg193008
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115539
Supporting Variants
Samplessample362
Known GenesC3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101499
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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