A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5558512



Internal ID331571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:207645319..207645535hg38UCSC Ensembl
chr2:208510043..208510259hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg38217
hg19217
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16924786
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5558512
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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