A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559405



Internal ID332439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:58205932..58213030hg38UCSC Ensembl
chr11:57973404..57980502hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg387099
hg197099
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17047044
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559405
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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