A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18281483



Internal ID20848523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93870508..93874875hg38UCSC Ensembl
chr9:96632790..96637157hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg384368
hg194368
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6562342
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18281483
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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