A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561523



Internal ID334501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:3128558..3135474hg38UCSC Ensembl
chr3:3170242..3177158hg19UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg386917
hg196917
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16929272
Samples
Known GenesTRNT1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561523
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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