A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18281168



Internal ID20848208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:81742613..81743547hg38UCSC Ensembl
chr9:84357528..84358462hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg38935
hg19935
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6557000
Supporting Variants
Samples
Known GenesLOC101927502
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18281168
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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