A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5419992



Internal ID199110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:91116999..91116999hg38UCSC Ensembl
chr15:91660229..91660229hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38275
hg19275
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17705139
Samples
Known GenesSV2B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5419992
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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