A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14281297



Internal ID22254645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:122499713..122581147hg38UCSC Ensembl
Outerchr9:125261992..125343426hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3881435
hg1981435
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3224054
Supporting Variants
SamplesNA19238
Known GenesOR1J2, OR1J4, OR1L8, OR1N1, OR1N2
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14281297
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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