A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3226913



Internal ID22369562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:19862861..19863550hg38UCSC Ensembl
chr16:19874183..19874872hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38690
hg19690
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14390981
SamplesHG00514
Known GenesGPRC5B
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3226913
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