A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5641734



Internal ID21590039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:8057750..8057750hg38UCSC Ensembl
chr5:8057863..8057863hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17143032
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5641734
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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