A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3206560



Internal ID22355079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:52167426..52167494hg38UCSC Ensembl
chr20:50783965..50784033hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14459912
SamplesHG00733
Known GenesZFP64
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3206560
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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