A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3227302



Internal ID22369837
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14281927, nssv14281928
SamplesNA19239, NA19240
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3227302
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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