A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18280992



Internal ID20848033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:75159915..75160173hg38UCSC Ensembl
chr9:77774831..77775089hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38259
hg19259
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6563948
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18280992
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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