A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6599906



Internal ID20972977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38659389..38659727hg38UCSC Ensembl
chr22:39055394..39055732hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254976
Samples
Known GenesCBY1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6599906
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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