A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5430177



Internal ID208994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:12495000..12502600hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg387601
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17727451
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5430177
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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