A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3563875



Internal ID22432611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:16590914..16590914hg38UCSC Ensembl
chr5:16591023..16591023hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14320358
SamplesNA19240
Known GenesFAM134B
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3563875
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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