A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6597956



Internal ID20971027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:19421157..19421842hg38UCSC Ensembl
chr22:19408680..19409365hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38686
hg19686
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254926
Samples
Known GenesHIRA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6597956
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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