A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3225884



Internal ID22368883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:31441319..31441370hg38UCSC Ensembl
chr8:31298835..31298886hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14340436, nssv14340437
SamplesHG00731, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3225884
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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