A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3198603



Internal ID22348306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:28312652..28312706hg38UCSC Ensembl
chr4:28314274..28314328hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6527n152
Supporting Variantsnssv14313244, nssv14313243
SamplesHG00512, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3198603
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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