A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5562885



Internal ID335826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:60447122..60474491hg38UCSC Ensembl
chr14:60913840..60941209hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg3827370
hg1927370
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17695964
Samples
Known GenesC14orf39
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5562885
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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