A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5661340



Internal ID21609645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55454258..55454258hg38UCSC Ensembl
chr19:55965625..55965625hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38672
hg19672
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17107021
SamplesHG03371
Known GenesISOC2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5661340
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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