A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5878402



Internal ID22653367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:93812288..93829148hg38UCSC Ensembl
chr15:94355517..94372377hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3816861
hg1916861
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474925
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5878402
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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