A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18263754



Internal ID20830794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:148683620..149348635hg38UCSC Ensembl
chr4:149604772..150269787hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg38665016
hg19665016
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6571486
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18263754
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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