A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101114



Internal ID21289092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:9166640..9179255hg38UCSC Ensembl
Innerchr19:9277316..9289931hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3812616
hg1912616
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113150
Supporting Variants
Samplessample43
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101114
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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