A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16255891



Internal ID21398338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18171404..18408694hg38UCSC Ensembl
chrUn_gl000212:156..186858hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38237291
hg19186703
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730259
Supporting Variants
SamplesHG00513
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16255891
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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