A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3201877



Internal ID22351117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:49972528..49976525hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg383998
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14456254, nssv14410182, nssv14410183, nssv14460989
SamplesNA19240, HG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3201877
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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