A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6092052



Internal ID22001285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:43561684..43561684hg38UCSC Ensembl
chr11:43583234..43583234hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17584740
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6092052
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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