A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6051210



Internal ID21960443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:16537885..16537885hg38UCSC Ensembl
chr3:16579392..16579392hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17549306
Samples
Known GenesLINC00690
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6051210
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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