A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5629928



Internal ID21578233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:130525317..130525317hg38UCSC Ensembl
chr10:132323581..132323581hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17068928
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5629928
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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