A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5665400



Internal ID21613705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:58097021..58097021hg38UCSC Ensembl
chr20:56672077..56672077hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg38531
hg19531
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17117495
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5665400
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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