A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6092688



Internal ID22001921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:19860131..19860131hg38UCSC Ensembl
chr11:19881677..19881677hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38187
hg19187
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17580101
Samples
Known GenesNAV2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6092688
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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