A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559193



Internal ID332234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:12625634..12679425hg38UCSC Ensembl
chr20:12606281..12660072hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3853792
hg1953792
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17730940
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559193
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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