A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6599692



Internal ID20972763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38892944..38894032hg38UCSC Ensembl
chr22:39288949..39290037hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg381089
hg191089
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254977
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6599692
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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