A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256105



Internal ID21398532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18215202..18357590hg38UCSC Ensembl
chrUn_gl000212:43954..186342hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38142389
hg19142389
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730259
Supporting Variants
SamplesHG00514
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256105
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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