A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565261



Internal ID20938332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:95359076..95359311hg38UCSC Ensembl
chr9:98121358..98121593hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38236
hg19236
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18281527
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565261
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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