A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5648859



Internal ID21597164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65802273..65802273hg38UCSC Ensembl
chr15:66094611..66094611hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17098824
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5648859
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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