A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14281928



Internal ID22326306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:80359553..80373738hg38UCSC Ensembl
Outerchr9:82974468..82988653hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg3814186
hg1914186
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3227302
Supporting Variants
SamplesNA19240
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14281928
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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