A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559777



Internal ID332800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:74222274..74233318hg38UCSC Ensembl
chr5:73518099..73529143hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg3811045
hg1911045
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16966884
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559777
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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