A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17706290



Internal ID129956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:27823433..27825113hg38UCSC Ensembl
chr16:27834754..27836434hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg381681
hg191681
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5558649
Supporting Variants
Samples
Known GenesGSG1L
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17706290
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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