A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257437



Internal ID21397956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:16450252..18258138hg38UCSC Ensembl
chr16:16544109..18351995hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg381807887
hg191807887
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730208
Supporting Variants
SamplesHG00512
Known GenesXYLT1
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257437
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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