A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16946649



Internal ID31792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:26813907..26846400hg38UCSC Ensembl
chr4:26815529..26848022hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3832494
hg1932494
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5555719
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16946649
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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