A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6068939



Internal ID21978172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:139114406..139114406hg38UCSC Ensembl
chr3:138833248..138833248hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17545459
Samples
Known GenesBPESC1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6068939
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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