A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5562784



Internal ID335728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:325118..325725hg38UCSC Ensembl
chr20:305762..306369hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38608
hg19608
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17730171
Samples
Known GenesSOX12
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5562784
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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