A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116988



Internal ID21300254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:9164276..9180468hg38UCSC Ensembl
Innerchr19:9274952..9291144hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3816193
hg1916193
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv548n145
Supporting Variantsnssv14101386
Samplessample314
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116988
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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