A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14370090



Internal ID22123606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:28905151..28910679hg38UCSC Ensembl
chr14:29374357..29379885hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg385529
hg195529
Variant TypeOTHER sequence alteration
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3243867
Supporting Variants
SamplesHG00512
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14370090
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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