A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3213773



Internal ID22360611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:62944669..65663532hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg382718864
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14439738, nssv14439212
SamplesHG00733, HG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3213773
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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