A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17703353



Internal ID127019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:95689449..95691493hg38UCSC Ensembl
chr15:96232678..96234722hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg382045
hg192045
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556281
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17703353
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000781


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