A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16895055



Internal ID170884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:211404548..211457277hg38UCSC Ensembl
chr1:211577890..211630619hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg3852730
hg1952730
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5559367
Supporting Variants
Samples
Known GenesLINC00467
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16895055
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.025921


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