A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6070849



Internal ID21980082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:179727879..179727879hg38UCSC Ensembl
chr3:179445667..179445667hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38184
hg19184
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17551515
Samples
Known GenesUSP13
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6070849
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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