A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5411484



Internal ID190791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:105525792..105525843hg38UCSC Ensembl
chr9:108288073..108288124hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17025095
Samples
Known GenesFSD1L
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5411484
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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