A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6080894



Internal ID21990127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:122769284..122769284hg38UCSC Ensembl
chr12:123253831..123253831hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17606537
Samples
Known GenesDENR
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6080894
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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