A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3208276



Internal ID22356545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:179727100..179728753hg38UCSC Ensembl
chr3:179444888..179446541hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg381654
hg191654
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14312034, nssv14312035, nssv14312036, nssv14312037
SamplesHG00512, HG00732, HG00513, HG00514
Known GenesUSP13
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3208276
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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