A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4761601



Internal ID20537461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:118248256..118248256hg38UCSC Ensembl
chr10:120007768..120007768hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16272229
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4761601
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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