A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3206034



Internal ID22354638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87758183..87758263hg38UCSC Ensembl
chr9:90373098..90373178hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14439553
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)nsv3206034
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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