A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3526881



Internal ID22396264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:48003033..48005435hg38UCSC Ensembl
chr1:48468705..48471107hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg382403
hg192403
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14365731, nssv14365730
SamplesNA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3526881
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