A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3563672



Internal ID22432408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:113585653..113585653hg38UCSC Ensembl
chr4:114506809..114506809hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14315570, nssv14315569
SamplesHG00731, HG00513
Known GenesCAMK2D
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3563672
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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