A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5654335



Internal ID21602640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60542566..60542566hg38UCSC Ensembl
chr15:60834765..60834765hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38534
hg19534
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17087816
SamplesHG03371
Known GenesRORA
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5654335
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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