A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6100299



Internal ID22009532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134037098..134037098hg38UCSC Ensembl
chr11:133906993..133906993hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17605275
Samples
Known GenesLOC100128239
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6100299
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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