A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3208177



Internal ID22356460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:35490480..35490689hg38UCSC Ensembl
chr22:35886473..35886682hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38210
hg19210
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14451261
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3208177
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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