A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18281357



Internal ID20848397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88518227..88520139hg38UCSC Ensembl
chr9:91133142..91135054hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg381913
hg191913
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6565223
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18281357
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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