A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6597594



Internal ID20970665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:21783190..21783559hg38UCSC Ensembl
chr22:22137479..22137848hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38370
hg19370
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253707
Samples
Known GenesMAPK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6597594
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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