A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257780



Internal ID21400090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14789461..14903187hg38UCSC Ensembl
chr16:14883318..14997044hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38113727
hg19113727
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730140
Supporting Variants
SamplesNA19238
Known GenesABCC6P2, MIR3179-1, MIR3179-2, MIR3179-3, NOMO1
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257780
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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