A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101902



Internal ID21266721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:29439659..29447199hg38UCSC Ensembl
Innerchr19:29930566..29938106hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg387541
hg197541
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117667
Supporting Variants
Samplessample101
Known GenesLOC284395
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101902
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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