A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114574



Internal ID21297840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:17542088..17567600hg38UCSC Ensembl
Innerchr4:17543711..17569223hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3825513
hg1925513
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv861n145
Supporting Variantsnssv14107382, nssv14107143, nssv14089305, nssv14107690
Samplessample7, sample48, sample111, sample99
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114574
Frequency
Sample Size467
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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