A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3208333



Internal ID22356593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130429628..130429712hg38UCSC Ensembl
chr9:133305015..133305099hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14437409
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)nsv3208333
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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