A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3196866



Internal ID22346809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:52444906..52444958hg38UCSC Ensembl
chr1:52910578..52910630hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv215n152
Supporting Variantsnssv14366761, nssv14366762, nssv14366763
SamplesNA19238, NA19239, NA19240
Known GenesZCCHC11
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3196866
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer