A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3561003



Internal ID22429797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:34904140..34904140hg38UCSC Ensembl
chr18:32484104..32484104hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14283365, nssv14283363, nssv14283364
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3561003
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