A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5536441



Internal ID311918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:82841056..82841104hg38UCSC Ensembl
chr11:82552098..82552146hg19UCSC 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 Variantsnssv17048089
Samples
Known GenesPRCP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5536441
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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