A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116041



Internal ID21299307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:36193688..36197534hg38UCSC Ensembl
Innerchr14:36662894..36666740hg19UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg383847
hg193847
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv324n145
Supporting Variantsnssv14095594, nssv14095442
Samplessample169, sample234
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116041
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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