A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5650227



Internal ID21598532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64046334..64046334hg38UCSC Ensembl
chr15:64338533..64338533hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17086702
SamplesHG02492
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5650227
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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