A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5884419



Internal ID22659401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:98082835..98085438hg38UCSC Ensembl
chr15:98626064..98628667hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg382604
hg192604
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17472431
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5884419
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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