A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5555719



Internal ID328869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:26813907..26846400hg38UCSC Ensembl
chr4:26815529..26848022hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3832494
hg1932494
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16946649
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5555719
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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