A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3216634



Internal ID22362569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:65179656..65182641hg38UCSC Ensembl
chr8:66091891..66094876hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg382986
hg192986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14342354, nssv14342353
SamplesNA19239, NA19240
Known GenesLINC00251
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3216634
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