A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3202232



Internal ID22351421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:42078746..42078796hg38UCSC Ensembl
chr21:43498855..43498905hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14451178
SamplesHG00733
Known GenesUMODL1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3202232
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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