A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3193800



Internal ID22344201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:10943625..10943735hg38UCSC Ensembl
chrUn_gl000241:19053..19163hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14396824
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3193800
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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