A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5558064



Internal ID331139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:185914578..185914689hg38UCSC Ensembl
chr3:185632366..185632477hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16944830
Samples
Known GenesTRA2B
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5558064
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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