A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16971875



Internal ID48603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:109325168..109325171hg38UCSC Ensembl
chr5:108660869..108660872hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg384
hg194
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5561225
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16971875
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.027943


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