A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6081378



Internal ID21990611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59645351..59645351hg38UCSC Ensembl
chr11:59412824..59412824hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17595275
Samples
Known GenesPATL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6081378
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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