A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256862



Internal ID21398095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:28402329..28736286hg38UCSC Ensembl
chr16:28413650..28747607hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38333958
hg19333958
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730105
Supporting Variants
SamplesHG00512
Known GenesAPOBR, CCDC101, CLN3, EIF3C, EIF3CL, IL27, MIR6862-1, MIR6862-2, NUPR1, SULT1A1, SULT1A2
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256862
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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