A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258833



Internal ID21398369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:16235688..18731328hg38UCSC Ensembl
chr16:16329545..18742650hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg382495641
hg192413106
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730208
Supporting Variants
SamplesHG00513
Known GenesABCC6P1, LOC100288162, MIR3179-1, MIR3179-2, MIR3179-3, MIR3180-1, MIR3180-2, MIR3180-3, MIR6511A-2, MIR6770-2, NOMO2, NOMO3, NPIPA7, NPIPA8, PKD1P1, XYLT1
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258833
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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