A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18266065



Internal ID20833105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:84359359..84360275hg38UCSC Ensembl
chr4:85280512..85281428hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg38917
hg19917
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6565108
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18266065
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00012


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