A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5510866



Internal ID287474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:84371367..84390135hg38UCSC Ensembl
chr13:84945502..84964270hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3818769
hg1918769
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17691465
Samples
Known GenesLINC00333
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5510866
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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