A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567440



Internal ID20940511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96626899..96627027hg38UCSC Ensembl
chr9:99389181..99389309hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18281568
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567440
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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