A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4332531



Internal ID19839095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:60897225..60985746hg38UCSC Ensembl
chr14:61363943..61452464hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg3888522
hg1988522
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15788150
Samples
Known GenesMNAT1, SLC38A6, TRMT5
MethodSequencing
AnalysisSV calls were generated using multi-algorithm consensus pipeline involving raw evidence assessment, filtering, clustering, genotyping, alternative allele structure resolution, and gene annotation. These methods are described in detail in the gnomAD-SV preprint [Collins*, Brand*, et al., bioRxiv (2019)|https://www.biorxiv.org/content/10.1101/578674v1], and are largely based on methods developed in [Werling et al., Nat. Genet. (2018)|https://www.ncbi.nlm.nih.gov/pubmed/29700473].
Platform
Commentscomplex variant
ReferencegnomAD_Structural_Variants
Pubmed ID12345678
Accession Number(s)nsv4332531
Frequency
Sample Size10847
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer