A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257202



Internal ID21397965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:28343932..28822601hg38UCSC Ensembl
chr16:28355253..28833922hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38478670
hg19478670
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, NPIPB6, NUPR1, SULT1A1, SULT1A2
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257202
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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