A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3222799



Internal ID22366765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:42365861..42365937hg38UCSC Ensembl
chr13:42939997..42940073hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14369584
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3222799
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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