A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17410821



Internal ID22468691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:158744603..158748924hg38UCSC Ensembl
chr3:158462392..158466713hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg384322
hg194322
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5979868
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17410821
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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