A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3207098



Internal ID22355546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:222487880..222488138hg38UCSC Ensembl
chr1:222661222..222661480hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38259
hg19259
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv568n152
Supporting Variantsnssv14308801, nssv14308802
SamplesNA19238, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3207098
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