A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111098



Internal ID21294364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:36192561..36197534hg38UCSC Ensembl
Innerchr14:36661767..36666740hg19UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg384974
hg194974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv323n145
Supporting Variantsnssv14093976, nssv14095409, nssv14095073, nssv14095621, nssv14095557
Samplessample218, sample291, sample244, sample160, sample339
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111098
Frequency
Sample Size467
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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