A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596234



Internal ID20969305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:35243169..35243738hg38UCSC Ensembl
chr22:35639162..35639731hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38570
hg19570
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18255195
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596234
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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