A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3563692



Internal ID22432428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:129291255..129291255hg38UCSC Ensembl
chr4:130212410..130212410hg19UCSC Ensembl
Cytoband4q28.2
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14315102, nssv14315103
SamplesNA19239, HG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3563692
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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