A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3239965



Internal ID22374573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:86984977..87015437hg38UCSC Ensembl
Outerchr9:89599892..89630352hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg381023
hg191023
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9639n152
Supporting Variantsnssv14253172
SamplesHG00731
Known GenesLOC100506834, LOC440173
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3239965
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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