A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4762039



Internal ID20537899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97305597..97305597hg38UCSC Ensembl
chr10:99065354..99065354hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg38n/a
hg19n/a
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16265910
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4762039
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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