A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17705139



Internal ID128805
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 StatusS
Merged Variantsnsv5419992
Supporting Variants
Samples
Known GenesSV2B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17705139
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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