A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5563584



Internal ID336516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:62290581..62361364hg38UCSC Ensembl
chr2:62517716..62588499hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg3870784
hg1970784
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16913871
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5563584
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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