A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3229718



Internal ID22371474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85911187..85911684hg38UCSC Ensembl
chr16:85944793..85945290hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38498
hg19498
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14372687, nssv14388790
SamplesHG00512, HG00513
Known GenesIRF8
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3229718
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