A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5883305



Internal ID22658284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:100352626..100361550hg38UCSC Ensembl
chr15:100892831..100901755hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg388925
hg198925
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17469971
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5883305
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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