A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14322035



Internal ID22283049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:90822114..90929330hg38UCSC Ensembl
chr5:90117931..90225147hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38107217
hg19107217
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3206296
Supporting Variants
SamplesNA19239
Known GenesGPR98
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14322035
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