A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3528510



Internal ID22397898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:83357214..83357277hg38UCSC Ensembl
chr9:85972129..85972192hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9626n152
Supporting Variantsnssv14347794, nssv14347793, nssv14347791, nssv14347792
SamplesHG00512, NA19238, NA19240, HG00514
Known GenesFRMD3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3528510
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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