A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3525516



Internal ID22394894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:16412278..16412614hg38UCSC Ensembl
chr4:16413901..16414237hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg38337
hg19337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14312336, nssv14312337, nssv14312333, nssv14312334, nssv14312335
SamplesHG00512, HG00732, NA19240, HG00733, HG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3525516
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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