A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3202561



Internal ID22351708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:93225187..93231370hg38UCSC Ensembl
chr8:94237416..94243599hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg386184
hg196184
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14377089
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)nsv3202561
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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