A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14305428



Internal ID22327711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15737522..15737522hg38UCSC Ensembl
chr3:15779029..15779029hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3563234
Supporting Variants
SamplesNA19240
Known GenesANKRD28
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14305428
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