A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18281197



Internal ID20848237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:82495006..82506096hg38UCSC Ensembl
chr9:85109921..85121011hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3811091
hg1911091
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6561445
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18281197
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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