A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14107653



Internal ID21292913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:108178749..108192135hg38UCSC Ensembl
Innerchr4:109099905..109113291hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3813387
hg1913387
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111537
Supporting Variants
Samplessample93
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14107653
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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