A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3227235



Internal ID22369795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:33576372..33576425hg38UCSC Ensembl
chr21:34948678..34948731hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5512n152
Supporting Variantsnssv14467257
SamplesHG00733
Known GenesSON
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3227235
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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