A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560324



Internal ID333334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:65688646..65688697hg38UCSC Ensembl
chr1:66154329..66154380hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg382852
hg192852
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16906133
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5560324
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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