A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5550228



Internal ID323807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:77012144..77012170hg38UCSC Ensembl
chr9:79627060..79627086hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17025914
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5550228
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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