A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5556590



Internal ID329725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:114305082..114307996hg38UCSC Ensembl
chr3:114023929..114026843hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg382915
hg192915
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16937994
Samples
Known GenesTIGIT
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5556590
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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