A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4767993



Internal ID20543853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:160409206..160409206hg38UCSC Ensembl
chr3:160126994..160126994hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg38163
hg19163
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288507
Samples
Known GenesSMC4
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4767993
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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