A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6062123



Internal ID21971356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:139527888..139527888hg38UCSC Ensembl
chr3:139246730..139246730hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17547476
Samples
Known GenesRBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6062123
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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