A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5638774



Internal ID21587079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:128195882..128195882hg38UCSC Ensembl
chr10:129994146..129994146hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17068706
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5638774
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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