A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561999



Internal ID334965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97692708..97692708hg38UCSC Ensembl
chr9:100454990..100454990hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17027577
Samples
Known GenesXPA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561999
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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