A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257635



Internal ID21399319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:18381565..18390527hg38UCSC Ensembl
chr16:18475422..18484384hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg388963
hg198963
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730208
Supporting Variants
SamplesHG00732
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257635
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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