A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5886099



Internal ID22661085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:93887844..93889343hg38UCSC Ensembl
chr15:94431073..94432572hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474932, nssv17474931
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5886099
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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