A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17707819



Internal ID131485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:48616897..48617438hg38UCSC Ensembl
chr16:48650808..48651349hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38542
hg19542
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563046
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17707819
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.369029


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