A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598833



Internal ID20971904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:18006741..18007005hg38UCSC Ensembl
chr22:18489507..18489771hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38265
hg19265
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254899
Samples
Known GenesMICAL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598833
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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