A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5979453



Internal ID22754388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:82841053..82841053hg38UCSC Ensembl
chr11:82552095..82552095hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17356550
Samples
Known GenesPRCP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5979453
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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