A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14092131



Internal ID21275122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:140009887..140014441hg38UCSC Ensembl
Innerchr4:140931041..140935595hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg384555
hg194555
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117861
Supporting Variants
Samplessample217
Known GenesMAML3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14092131
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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