A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6599608



Internal ID20972679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:31709510..31711649hg38UCSC Ensembl
chr22:32105496..32107635hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg382140
hg192140
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18255110
Samples
Known GenesPRR14L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6599608
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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