A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17026915



Internal ID85665
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 StatusS
Merged Variantsnsv5401458
Supporting Variants
Samples
Known GenesLPPR1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17026915
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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