A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18281560



Internal ID20848600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96546448..96546993hg38UCSC Ensembl
chr9:99308730..99309275hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38546
hg19546
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6557631
Supporting Variants
Samples
Known GenesCDC14B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18281560
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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