A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5979677



Internal ID22754612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:81163208..81163208hg38UCSC Ensembl
chr15:81455549..81455549hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38187
hg19187
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17386644
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5979677
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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