A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527620



Internal ID22397007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76098396..76098470hg38UCSC Ensembl
chr18:73810351..73810425hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3931n152
Supporting Variantsnssv14287208, nssv14287207
SamplesHG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527620
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