A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14281166



Internal ID22199569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:69273490..69296263hg38UCSC Ensembl
Outerchr9:71888406..71911179hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3822774
hg1922774
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3213028
Supporting Variants
SamplesHG00732
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14281166
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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