A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3526322



Internal ID22395702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:230315348..230315456hg38UCSC Ensembl
chr1:230451094..230451202hg19UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14312481, nssv14312482
SamplesNA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3526322
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