A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5664179



Internal ID21612484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92875120..92875120hg38UCSC Ensembl
chr15:93418350..93418350hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17092550
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5664179
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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