A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5401458



Internal ID180835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:101123126..101123177hg38UCSC Ensembl
chr9:103885408..103885459hg19UCSC Ensembl
Cytoband9q31.1
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 Variantsnssv17026915
Samples
Known GenesLPPR1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5401458
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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