A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3201192



Internal ID22350535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:5214507..5214560hg38UCSC Ensembl
chr1:5274567..5274620hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv77n152
Supporting Variantsnssv14298014, nssv14298013
SamplesHG00731, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3201192
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