A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527210



Internal ID22396596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:70813493..70813637hg38UCSC Ensembl
chr14:71280210..71280354hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg38145
hg19145
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14371151, nssv14371150
SamplesHG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527210
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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