A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16890889



Internal ID168103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156338639..156344748hg38UCSC Ensembl
chr1:156308430..156314539hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg386110
hg196110
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5559729
Supporting Variants
Samples
Known GenesTSACC
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16890889
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000937


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