A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5558052



Internal ID331127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:104368774..104375354hg38UCSC Ensembl
chr12:104762552..104769132hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg386581
hg196581
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17690526
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5558052
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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