A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5564090



Internal ID337012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:14092969..14105333hg38UCSC Ensembl
chr3:14134469..14146833hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3812365
hg1912365
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16930481
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5564090
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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