A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112978



Internal ID21296244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:98657555..98663357hg38UCSC Ensembl
Innerchr4:99578706..99584508hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg385803
hg195803
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14092119
Samplessample214
Known GenesTSPAN5
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112978
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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