A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5502312



Internal ID279184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24411965..24412056hg38UCSC Ensembl
chr14:24881171..24881262hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17693439
Samples
Known GenesNYNRIN
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5502312
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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