A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257618



Internal ID21398274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:18122626..18256440hg38UCSC Ensembl
chr16:18216483..18350297hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38133815
hg19133815
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730208
Supporting Variants
SamplesHG00513
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257618
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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