A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5556673



Internal ID329804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:99387035..99387271hg38UCSC Ensembl
chr15:99927240..99927476hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38237
hg19237
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17705286
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5556673
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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