A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17708926



Internal ID132592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89926006..90098466hg38UCSC Ensembl
chr16:89992414..90164874hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38172461
hg19172461
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5560018
Supporting Variants
Samples
Known GenesAFG3L1P, C16orf3, CENPBD1, DBNDD1, DEF8, GAS8, PRDM7, TUBB3, URAHP
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17708926
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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