A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5864241



Internal ID22639176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65136432..65137831hg38UCSC Ensembl
chr15:65428770..65430169hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17473534, nssv17473533
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5864241
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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