A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3206833



Internal ID22355319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:128646527..128646585hg38UCSC Ensembl
chr8:129658773..129658831hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14453005
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)nsv3206833
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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