A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595811



Internal ID20968882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:34273423..34274782hg38UCSC Ensembl
chr22:34669413..34670772hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg381360
hg191360
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4692n223
Supporting Variantsnssv18255177
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595811
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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