A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3538751



Internal ID22407927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:17409213..17410033hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38821
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14302972, nssv14302971, nssv14302970
SamplesHG00731, HG00732, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3538751
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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