A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18265499



Internal ID20832539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:98960559..98961082hg38UCSC Ensembl
chr4:99881710..99882233hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg38524
hg19524
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6569481
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18265499
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00038


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