A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113659



Internal ID21296925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:17542088..17567072hg38UCSC Ensembl
Innerchr4:17543711..17568695hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3824985
hg1924985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv861n145
Supporting Variantsnssv14094952, nssv14096594, nssv14094678, nssv14107188, nssv14096634
Samplessample413, sample421, sample400, sample17, sample357
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113659
Frequency
Sample Size467
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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