A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14371981



Internal ID22262107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:76231963..76231963hg38UCSC Ensembl
chr14:76698306..76698306hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3560420
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14371981
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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