A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3223030



Internal ID22366918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:124437553..124457509hg38UCSC Ensembl
Outerchr9:127199832..127219788hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3819957
hg1919957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14281298
SamplesNA19238
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3223030
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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