A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14107624



Internal ID21292417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:166343145..166395480hg38UCSC Ensembl
Innerchr4:167264297..167316632hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3852336
hg1952336
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111570
Supporting Variants
Samplessample88
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14107624
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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