A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14304637



Internal ID22133123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:10873400..10873552hg38UCSC Ensembl
chr3:10915085..10915237hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV duplication
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3526060
Supporting Variants
SamplesHG00513
Known GenesSLC6A11
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14304637
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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