A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18280205



Internal ID20847245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15340721..15345984hg38UCSC Ensembl
chr9:15340719..15345982hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg385264
hg195264
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6574084
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18280205
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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