A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4761133



Internal ID20536993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:129249493..129249493hg38UCSC Ensembl
chr10:131047757..131047757hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16289247
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4761133
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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