A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6092560



Internal ID22001793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134055477..134055477hg38UCSC Ensembl
chr11:133925372..133925372hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38159
hg19159
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17607555
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6092560
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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