A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6081399



Internal ID21990632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:75877877..75877877hg38UCSC Ensembl
chr11:75588921..75588921hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17595437
Samples
Known GenesUVRAG
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6081399
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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