A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3205989



Internal ID22354602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:12039810..12043159hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg383350
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14434038, nssv14434039
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3205989
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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