A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3564106



Internal ID22432841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:8609062..8609062hg38UCSC Ensembl
chr4:8610789..8610789hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14311385, nssv14311386, nssv14311387
SamplesHG00731, HG00732, HG00733
Known GenesCPZ
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3564106
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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