A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3203893



Internal ID22352835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:47732664..47732722hg38UCSC Ensembl
chr22:48128413..48128471hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14423362
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)nsv3203893
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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