A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5541987



Internal ID316490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:101238295..101238295hg38UCSC Ensembl
chr9:104000577..104000577hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17026919
Samples
Known GenesLPPR1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5541987
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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