A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595954



Internal ID20969025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:33751197..33751959hg38UCSC Ensembl
chr22:34147184..34147946hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38763
hg19763
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18255165
Samples
Known GenesLARGE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595954
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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