A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3215437



Internal ID22361776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:79287499..79297442hg38UCSC Ensembl
Outerchr9:81902414..81912357hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg389944
hg199944
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14282901
SamplesHG00731
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3215437
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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