A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18265492



Internal ID20832532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:98873801..98874454hg38UCSC Ensembl
chr4:99794952..99795605hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg38654
hg19654
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6565459
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18265492
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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