A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6061681



Internal ID21970914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:177457361..177457361hg38UCSC Ensembl
chr3:177175149..177175149hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17543397
Samples
Known GenesLINC00578
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6061681
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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