A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5541783



Internal ID316340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24406247..24406254hg38UCSC Ensembl
chr14:24875453..24875460hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17693438
Samples
Known GenesNYNRIN
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5541783
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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