A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5417981



Internal ID197163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:47456314..47456365hg38UCSC Ensembl
chr15:47748511..47748562hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17701208
Samples
Known GenesSEMA6D
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5417981
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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