A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6599140



Internal ID20972211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:30065147..30066927hg38UCSC Ensembl
chr22:30461136..30462916hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg381781
hg191781
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18255524
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6599140
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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