A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3223663



Internal ID22367361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:85806698..85823937hg38UCSC Ensembl
Outerchr9:88421613..88438852hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3817240
hg1917240
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14281930, nssv14281929
SamplesNA19239, NA19240
Known GenesLOC389765
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3223663
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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