A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5430994



Internal ID209785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:7620890..7626890hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg386001
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17733817
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5430994
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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