A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14107540



Internal ID21291600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:70926414..70932824hg38UCSC Ensembl
Innerchr4:71792131..71798541hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg386411
hg196411
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114453
Supporting Variants
Samplessample77
Known GenesMOB1B
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14107540
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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