A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6102266



Internal ID22011502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16022739..16022739hg38UCSC Ensembl
chr19:16133549..16133549hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17635727
Samples
Known GenesLINC00661
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6102266
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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