A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5879721



Internal ID22654693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:97358111..97378422hg38UCSC Ensembl
chr15:97901341..97921652hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3820312
hg1920312
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474968
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5879721
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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