A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14388461



Internal ID22273009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:97221511..97221565hg38UCSC Ensembl
chr14:97687848..97687902hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3221833
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14388461
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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