A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6079393



Internal ID21988626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:167446531..167446531hg38UCSC Ensembl
chr3:167164319..167164319hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17545933
Samples
Known GenesSERPINI2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6079393
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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