A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5502990



Internal ID279839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24274165..24318169hg38UCSC Ensembl
chr14:24743371..24787375hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3844005
hg1944005
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17693432
Samples
Known GenesCIDEB, DHRS1, LTB4R, LTB4R2, NOP9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5502990
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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