A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5564084



Internal ID337006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:39684363..39684401hg38UCSC Ensembl
chr15:39976564..39976602hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38355
hg19355
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17700087
Samples
Known GenesFSIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5564084
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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