A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3205822



Internal ID22354456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:92290774..92290998hg38UCSC Ensembl
chr9:95053056..95053280hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38225
hg19225
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14460082
SamplesHG00733
Known GenesIARS
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3205822
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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