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
hg38299
hg19299
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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