A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559888



Internal ID332908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:51133550..51227402hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3893853
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16981830
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559888
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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