A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6098644



Internal ID22007877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:20194458..20194458hg38UCSC Ensembl
chr11:20216004..20216004hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17587529
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6098644
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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