A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17693438



Internal ID117104
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 StatusS
Merged Variantsnsv5541783
Supporting Variants
Samples
Known GenesNYNRIN
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17693438
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0052


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