A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256122



Internal ID21398538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:28342684..28652009hg38UCSC Ensembl
chr16:28354005..28663330hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38309326
hg19309326
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730105
Supporting Variants
SamplesHG00514
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)nssv16256122
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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