A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565293



Internal ID20938364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:3749858..3816591hg38UCSC Ensembl
chr9:3749858..3816591hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg3866734
hg1966734
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18280676
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565293
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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