A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3200282



Internal ID22349758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15832341..15832744hg38UCSC Ensembl
chr6:15832572..15832975hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38404
hg19404
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7755n152
Supporting Variantsnssv14327555, nssv14327557, nssv14327556
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3200282
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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