A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257667



Internal ID21399777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14790200..15327894hg38UCSC Ensembl
chr16:14884057..15421751hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38537695
hg19537695
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730140
Supporting Variants
SamplesHG00733
Known GenesABCC6P2, LOC100288162, MIR3179-1, MIR3179-2, MIR3179-3, MIR3180-1, MIR3180-2, MIR3180-3, MIR3180-4, MIR6511A-2, MIR6511B-1, MIR6770-2, NOMO1, NPIPA1, NTAN1, PDXDC1, RRN3
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257667
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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