A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5556354



Internal ID329493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:30045271..30047962hg38UCSC Ensembl
chr3:30086762..30089453hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg382692
hg192692
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16931374
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5556354
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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