A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865479



Internal ID22640414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66573898..66575923hg38UCSC Ensembl
chr15:66866236..66868261hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg382026
hg192026
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17473550
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865479
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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