A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3227201



Internal ID22369767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36073886..36074454hg38UCSC Ensembl
chr21:37446184..37446752hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg38569
hg19569
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14301949, nssv14301947, nssv14301946, nssv14301948
SamplesHG00512, NA19239, HG00731, HG00733
Known GenesLOC100133286
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3227201
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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