A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5548899



Internal ID322611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:13387036..13387073hg38UCSC Ensembl
chr11:13408583..13408620hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17041343
Samples
Known GenesARNTL
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5548899
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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