A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3206191



Internal ID22354772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:236934058..236938343hg38UCSC Ensembl
chr1:237097358..237101643hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg384286
hg194286
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14315449, nssv14315448
SamplesHG00731, HG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3206191
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